Bureau Circular 5 S 1997

Republic of the Philippines
Department of Health
BUREAU OF FOOD AND DRUGS
Civic Drive, Filinvest
Alabang, Muntinlupa City
March 19, 1997

BUREAU CIRCULAR
No. 05 s. 1997
TO
: ALL DRUG ESTABLISHMENTS AND PARTIES CONCERNED
SUBJECT
: REVISED CHECKLIST OF REQUIREMENTS AND THE 1997

GUILDELINES
FOR
THE
REGISTRATION
OF
PHARMACEUTICAL PRODUCTS
The BFAD has adopted the 1997 Guidelines for the Registration of Pharmaceutical Products
and has revised the checklist of requirements according to the said guidelines. Copies of the 1997
Guidelines etc. and the Revised Checklist of Requirements are attached as Annex A and B
respectively.
Hence, effective April 1, 1997, all applications for products registration shall be contained in
the PSD application form (PSD Form No. 8) and together with the submitted requirements as listed in
the checklist, shall be pre-assessed and submitted at the Public Assistance, Information and
Compliance Section in accordance with the 1997 Guidelines for Registration of Pharmaceutical
Products.
Any application that will not comp pharmaceutically with the said guidelines shall be returned
to the applicant and may be re-submitted only after the completion of the requirements.
(Sgd) QUINTIN L. KINTANAR, M.D., Ph.D.

Director
ANNEX B
1997 GUIDELINES FOR THE REGISTRATION OF
PHARMACEUTICAL PRODUCTS
I.
INTRODUCTION
These guidelines are formulated to guide the pharmaceutical companies in the preparation
and submission of drug registration applications and as an aid for the Bureau of Food and
Drugs - Product Services Division (BFAD-PSD) evaluators in assessing the acceptability of
such applications as well as the approval of registration of the product applied for.
A correctly accomplished application form and well-arranged with complete documentation
facilitate the work of the evaluators and can contribute to shorten the time required for the
evaluation of applications for registration. All pertinent documents and information regarding
the product shall be fully disclosed as these shall be used as bases in evaluating the
acceptability of the drug product for registration.
1.1.
DRUG REGISTRATION
The main function of the regulatory agency on pharmaceuticals is to ensure that all
drug products being made available to the general public are safe, efficacious and of
good quality.
Registration of drug products as required by RA 3720 as amended enables the BFAD
to assess the benefits of a product complying with the criteria of safety, efficacy and
good quality and to control or regulate its distribution.
All products which fall under the definition of drugs are required to be registered
following the procedure and requirements stated in this guidelines.
If all the criteria and requirements for registration have been met all applications
undergoing final evaluation are issued an approval of registration whose validity
period is as follows:
1. Initial registration of drugs for general use shall be issued either 2 years or 5
years validity based on the application of the company.
2. Drugs which fall under the new drug monitored release category shall be given 3
years registration validity.
3. Renewal registrations are valid for 5 years.
If any of the requirements are not met, a letter shall be sent to the
company denying the application. An application for reconsideration shall no longer
be allowed but the application may submit an application for initial registration for the
same product correcting all deficiencies.
1.2.
DRUG EVALUATION
The evaluation of drug product is primarily a process to determine its safety, efficacy
and quality.
Safety means that the drug product will not cause unfavorable reactions when used
according to its declared indication and that it does not have unexpected toxic
properties.
Efficacy pertains to a drug products ability to deliver the desired effect. It may be
expressed in terms of the extent of prevention or treatment of disease in man or the
manner in which it affects the structure or any function of the body of man or animals.
Quality as applied to a drug product requires that the product contains the quantity of
active ingredient(s) claimed on its label within the applicable limits of its specification.
It also means that the drug product can maintain its appearance, potency and
therapeutic availability until its claimed shelf-life/expiration.
All applications shall undergo a detailed evaluation of documents at the PSD and this
includes:
a. Complete formulation, facilities and methods of manufacture
b. Technical specifications, methods and results of quality control tests and analysis
conducted on all starting materials as well as on the in-process and finished
product
c. Complete data on stability testing and predicted shelf-life, container
description/specifications and recommended storage conditions
d. Labels or specimens of the proposed labels and other labeling materials such as
inserts, brochures, etc.
The application shall be accompanied by samples which shall be forwarded to the
Laboratory Services Division (LSD) for analysis which includes potency, identification
and other test requirements. The results of analysis on the samples shall be
forwarded to the PSD for final evaluation.
At any stage in the evaluation process an abeyance letter may be issued containing
questions and deficiencies regarding the product application.
2.
FILING OF APPLICATION FOR REGISTRATION

Only duly licensed pharmaceutical manufacturer, trader or distributor-importer/exporter may
file an application for registration of a drug product. A distributor-wholesaler cannot file an
application for registration.
The application submitted shall include a covering letter, a duly accomplished application form
(PSD Form No. 8) and complete requirements as listed in the checklist of requirements for
registration of pharmaceutical products. It is essential that the application shall be in
accordance with this guidelines.
Applications for registration of pharmaceutical products are accepted according to the
following schedule:
Company names starting with the letters A - E
F-M
N-Q
R-Z
Tuesday
Wednesday
- a.m.
- p.m.
- a.m.
- p.m.
A pre-assessment of the application shall be conducted by a PSD evaluator at the PAICS

(Public Assistance Information and Compliance Section). Only applications complying with all
registration requirements shall be accepted and processed.
3.
REQUIREMENTS FOR INITIAL REGISTRATION

3.1 ESTABLISHED DRUG
3.1.1
Application Letter
The Application/covering letter shall provide the following information
1. Name of the product
2. Dosage strength and dosage form
3. Name of the manufacturer, trader and distributor-importer/exporter, if
applicable
3.1.2
Certificate of Brand Name Clearance

Every brand name of a drug or pharmaceutical specialty shall be submitted
for name clearance prior to filing of application for registration. This will
prevent similarity in brand names with other previously registered drug
products or with the International Non-Proprietary Names (INN)
No imported drug or pharmaceutical specialty even if it is patented and/or
registered in other countries, shall be registered if there exists an identical or
similar brand name already registered with BFAD.
Application, processing and approval of brand names shall be in accordance
with the provisions of the following regulations:
1. Administrative Order No. 76 s. 1984
2. BFAD Regulation No. 2 s. 1986
3. Memorandum Circular No. 16-A s. 1994
3.1.3
Agreement between
Importer/Exporter
Manufacturer
and
Trader
or
Distributor-
The licensed trader or distributor shall submit a copy of valid agreement with
a BFAD-licensed manufacturer or a foreign manufacturer containing the
following:
-
3.1.4
the specific activity(ies) that each shall undertake relating to the

manufacture
a stipulation that both the manufacturer and trader/distributorimporter/exporter are jointly responsible for the quality of the product.
General Information
A detailed information regarding the product shall include the following:
- products proprietary or brand name
- official chemical name(s) and generic name(s) of active ingredient(s)
- molecular or chemical formula and structure
- amount of active ingredient per unit dose
- pharmaceutical form of the drug
- indication
- recommended dosage
- frequency of administration
- route and mode of administration
- contraindication
- warnings and precautions
3.1.5
Unit dose and batch formulation

A complete list of names and quantities of all active and non-active
ingredients shall be stated per unit dose (ex. per tablet) and per regular batch
production size (ex. per 100,000 tablets). The names and quantities of all
active ingredients shall be listed first followed by the non-active ingredients.
Ingredients which are incorporated in the formulation but which may
disappear during the production process (ex. alcohol, water) shall be included
in the list.
Overages must be indicated in quantitative terms and the reasons for them
are to be tested. Overages will usually not be acceptable unless it is proved
that they are necessary to achieve a reasonable shelf-life, or to compensate
for production losses.
3.1.6
Technical/Quality Specification of all Raw Material(s)

A complete technical/quality specifications and methods of analysis of all
starting materials shall be submitted. The quality specifications claimed shall
be those which are applied by the manufacturer in his own control
procedures. These shall include all requirements and test methods applied as
a routine to every batch. The description of the test methods shall be detailed
enough to enable the test to be carried out in an independent laboratory
The technical/quality specifications of each raw material must be presented in
separate lists comprising all test applied with the corresponding requirements
or test limits. These specifications shall be dated and signed by a person in
charge.
3.1.6.1 Ingredients
(Active
pharmacopoeia
or
Non-Active)
described
in
The current edition of the United States Pharmacopoeia/National

Formulary (USP/NF) is the official reference book adopted by the
BFAD for substances and articles used in the preparation of
pharmaceutical products. Reference to other national pharmacopoeia
such as the British Pharmacopoeia (B.P.), European Pharmacopoeia
(E.P) and the Japanese Pharmacopoeia (J.P) shall be considered if
the product has been sourced from countries where such
pharmacopoeia are official.
For substances which are subject of an official monograph, a concise
presentation of all tests applied with the corresponding requirements
or test limits shall be acceptable. The name and edition of the
pharmacopoeia being referred may be cited in lieu of stating the
detailed analytical producers.
In cases where different procedures are used in place of that
described in an official monograph, the technical/quality
specifications provided by the alternative procedure may be used but
shall not be any less stringent than that of the official monograph.
3.1.6.2 Ingredients (Active
pharmacopoeia
or
Non-Active)
not
described
in
The technical/quality specifications of ingredients not described in

any pharmacopoeia shall be presented in the form of a monograph
as follows:
1. The name of the substance supplemented by any trade or
scientific synonyms
2. Data relevant to the proof or evidence of molecular structure.
Detailed information on physical and chemical properties (e.g.
Isomerism). Emphasis should be placed on solubility, crystalline
form, particle size and state of hydration of state of other crystal
solvents. Other physical properties to be described are
polymorphism, hygroscopicity, melting point, boiling point,
density, viscosity, pKa., oil/water partition coefficient, etc.
3. Methods of identification may be described in the form of
complete techniques as used for production of the substance,
and in the form of tests which ought to be carried out as a routine
matter;
4. Purity tests shall be described in relation to the sum total of
predictable impurities, especially those which may have a
harmful effect and if necessary; those which, having regard to the
combination of substances to which the application refers, might
adversely affect the stability of the medicinal product or distort

analytical results.
3.1.6.3 Packaging Materials
Information shall be provided on the construction of the container,
with a list of the different components, the type of materials used in
the different parts, and the nature of the polymers. If the official
standards/pharmacopoeia include requirements concerning the type
of material used, it must be documented that these requirements will
be complied with (e.g. Glass bottles for parenteral solution). This also
applies to materials for accessories (infusion sets, syringes,
measuring devices).
For plastics, the name of material, name of the manufacturer,
chemical structure, and physico-chemical properties shall be
presented. For polymers intended for containers of liquid and semiliquid medicines, appropriate detailed information must be provided.
Complete composition, including possible polymerization residues,
stabilizers, plasticizers, colouring agents etc., shall be stated. The
maximum permitted content shall be indicated. A report on toxicity
may be required. Technical properties of the material relevant to the
proposed use shall be stated (sterilizability, permeability,
transparency, resistance etc.)
Detailed information is required about the technical construction of
non-standardized containers, e.g. aerosol containers, spray packs,
syringes etc.
3.1.7
Certificate of Analysis of Active Ingredient(s)

Validated and certified copies of the Certificate of Analysis from the supplier
of the active ingredient(s) shall be included in any submission.
The certificate(s) shall:
a. Be in English
b. Be on a letterhead or other paper that adequately identifies the company
manufacturing the materials.
c. Name of the material to which it refers and identify it by a batch number.
The batch number shall refer to the active material used in the
manufacture of the sample submitted for analyses
d. Be dated with the date of analyses and signed by a company officer over
his/her typewritten name
e. State the specifications (e.g. USP XXIII, BP 1993) and methods against
which and by which the tests are performed. These shall include all the
requirements stated in the technical/quality specifications document.
f. Give the test results (all tests and analyses that involve measurement
shall be reported as the actual numerical results, not description like
complies or pass).
Signed photocopies of such documents are acceptable as is a computer
generated document meeting the above requirements.
There is no objection to indicating besides any test result (or as a
footnote) that the test is equivalent to or more stringent than a
corresponding compendial test of specification, when this is scientifically
accurate.
3.1.8
Technical/Quality Specifications of Finished Product

The technical/quality specifications shall include all requirements and test
methods routinely applied to every batch. Requirements shall apply
throughout the shelf-life of the product. Information on requirements and test
not routinely applied to every batch shall be provided if they are of
importance to uniformity of quality as determined by the applicant company
or by the BFAD-PSD.
Information shall be furnished about the following:
a. The appearance of the product (colour, shape dimensions, odour,
distinguishing features, etc.)
b. Identification of the active ingredient(s) (must include the specific identity
test for the active moiety)
c. Quantitative determination of active ingredient(s) (i.e. Assay)
d. Test of impurities
e. The appropriate tests concerning the pharmaceutical properties of the
dosage form (e.g. pH, content uniformity, dissolution rate, disintegration,
etc)
f. Tests for safety, sterility, pyrogens, histamine, abnormal toxicity, etc.
where applicable.
g. Technical properties of containers
For drug preparations which are subject of an official monograph, the
technical/quality specifications of the finished product as stated in the
monograph shall be complied with.
3.1.9
Certificate of Analysis of the Finished Product

The Certificate of Analysis of the Finished Product shall include the results of
all the requirements and test methods stated in the technical/quality
specification of the product.
The Certificate, validated and certified, shall:
1. Refer to the same batch/lot number of the sample submitted for analyses
2. Be in English
3. Be on a letterhead or other copy that adequately identifies the
manufacturer of the product.
4. Be dated with the date of analyses and signed by a company officer over
his/her typed name
5. State the specifications and methods against which and by which the
tests are performed.
6. Give the test results (all tests and analyses that involve measurement
shall be reported as the actual numerical results, not descriptions like
"complies" or "pass"). In addition, for products requiring dissolution
testing, raw data shall be submitted for those described in a
pharmacopoeia and for those not described, the calculations shall also
be included.
7. Certificate of Analysis for finished products imported in bulk
Signed photocopies of such documents are acceptable as is a computer
generated document meeting the above requirements.
3.1.10 Full description of the methods used, the facilities and controls in the
manufacture, processing and packaging of the finished product.
A complete and detailed description of the manufacturing procedure including
all the facilities and equipment used in each stage of the manufacturing
process shall be given so that an assessment can be made of whatever the
processes employed in producing the pharmaceutical form might have
produced an adverse drug change in the constituents.
In case of continuous manufacture, full details concerning precautions taken

to ensure the homogeneity of the finished product shall be given. The actual
manufacturing formulation, with the quantitative particulars of all the
substances used shall be indicated. Mention shall also be made of any
substance that may be removed in the course of manufacture and any
overage shall be indicated and justified. Justification shall be submitted to
evaluation and may either be accepted or denied.
Stages of manufacture at which sampling for in-process controls such as
weight checks of tablets, homogeneity of suspensions, pH of solutions during
mixing and filling shall be indicated. Where a non-standard method of
manufacture is used or where it is critical for the product. Experimental
studies validating the manufacturing process shall be given. The
experimental studies shall likewise be subject to review or confirmation upon
evaluation of BFAD-PSD.
For drugs which must be aseptically prepared and sterile a detailed
description of the production process is required. This shall include data on
how sterilization is carried out and controlled. In some cases, e.g. for
aseptically prepared drugs, data must be provided on the microbiological
quantity or raw material specification and the property of the filter aid. (Refer
to M.C. _ s. 1996 for the Requirements for the Registration of Sterile
Products)
For products imported in bulk and repacked locally by a manufacturer,
identification and assay of active ingredient(s) shall be conducted prior to
repacking.
3.1.11 Details of the assay and other test procedures of finished product
including data analysis
Certain tests of the general characteristics of a product shall always be
including among the tests on the finished product. These tests shall,
wherever applicable, related to the control of average masses and maximum
deviations, to mechanical, physical or microbiological tests, organoleptic
characteristics, physical characteristics such as density, pH, refractive index,
etc. For each of these characteristics, standards and tolerance limits shall be
specified.
Identification and assay of the active ingredient(s) shall be carried out either
in a representative sample from the production batch or in a number of
dosage-unites analyzed individually.
Assay conducted at intermediate stages in the production process of
multicomponent drug products shall be acceptable on any one of the
following conditions:
a. Assay of the active components in the finished product will require an
intricate procedure.
b. Active ingredients are present in very low amounts.
Whenever necessary or whenever reports on its use shall pause danger to
the general public, the excipient(s) shall be subject at least to identification
test.
Identification tests and assay of preservatives and antioxidants must also be
included.
3.1.12 Detailed report of stability studies to justify claimed shelf-life

The manufacturer shall provide evidence to the effect that the product retains
acceptable strength and pharmaceutical quality throughout its shelf life. In
view of the fact that sufficiently long experience of storage of new products
has often not accumulated when an application is made, the results of
accelerated tests may be accepted for a preliminary shelf life, together with
previous experience of similar products. The manufacturer must, however,
outline his programme for further stability tests and will be required to report
results for several batches, covering the entire shelf-life. Stability of the
product must be followed up at a suitable frequency in relation to its shelf life,
a suitable number of regularly produced batches being tested. Changes in
composition, or the manufacturing process, or container and packaging
material may necessitate renewed investigations and a revised shelf life.
Conceivable changes in the chemical, pharmaceutical and biological
properties of the product during storage must be described. Changes in
concentrations of preservative(s) or antioxidant(s) and changes due to
interaction with the container must also be considered.
Information on the stability programme must include details of the number of
batches included, their composition, containers, the parameters studied (e.g.
content of active ingredient(s), degradation product(s), preservatives,
antioxidants, disintegration and/or dissolution, suspension stability, particle
size, etc), storage conditions testing intervals, etc. analytical methods must
be stated, supplemented with documentation of their ability to detect possible
changes. Special attention shall be given too the possibility of potentially
harmful or otherwise biologically active products forming.
Results shall be presented in an illustrative form, tables and graphs. In
addition, reports must specify the initial values, storage conditions, type of
container and batch number. Based on this, the manufacturer shall propose a
period of validity (shelf life) and if necessary any storage directions
applicable to distributors and consumers. (Refer to Annex GUIDELINES ON
THE STABILITY TESTING OF PHARMACEUTICALS)
3.1.13 Labels or specimens of the proposed label and other labeling materials
such as inserts, brochures, etc.
Requirements for the labeling of pharmaceutical products shall be in
accordance with the provisions of the following regulations:
Administrative Order No. 55 s. 1988 (as amended)
Administrative Order No. 85 s. 1990
Administrative Order No. 99 s. 1990
Memorandum Circular No. 6 s. 1991
Drug products shall be granted an exemption from generic labeling
requirements under any of the following categories:
1. Service Item
These shall include products which shall be available only on a limited
basis upon physicians request
2. Specially packed
These shall include products with special containers that cannot be made
and packed locally
3. Low volume of importation
These shall include products whose volume of importation shall not
exceed 500 units/month or 6,000 units/year
4. The drug product applied for requires special handling.

(e.g. biologicals which must always be refrigerated)
The company applying for generic labeling exemption shall submit together
with his application the following:
1. A copy of the subject products valid CPR. In case the product is still
undergoing registration process, the application may submit photocopies
of the application letter of registration and Official Receipt duly stamped
as received by BFAD-PAICS.
2. A representative sample including box and package insert of the product
requested for an exemption reflecting pertinent information such as
complete name and address of manufacturer and distributor/trader,
batch/lot number, manufacturing and expiry dates, Rx symbol, caution
and DR number.
3. A facsimile of the proposed generic labelling materials (immediate label,
box, package insert, etc.) for BFAD file.
3.1.14 Samples in market of commercial presentation
Samples of laboratory analysis shall be taken at random from an actual
production batch and packaged in the same container-closure system that
will be used for commercial purpose.
Samples shall be sufficient for use in assessing the products conformity with
the given test specifications plus sufficient retention sample for future
reference.
3.1.15 Duly authenticated Certificate of Free Sale from the country of origin
The Free Sale Certificate shall be issued by the regulatory agency on
pharmaceuticals from the drug products country of origin. It shall contain,
among others, the following information: The proprietary name or brand
name of the drug product, the generic name of International Non-Proprietary
Name (INN) of the active ingredient(s); the dosage strength & dosage form;
the complete name and address of the manufacturer and any other agency
which claims responsibility for the product. The Certificate shall also contain a
statement that the product is freely sold to the public.
In case the drug product is not freely sold in the country where it is
manufactured, an Export Certificate issued by the regulatory agency on
pharmaceuticals from the drug products manufacturer and a Free Sale
Certificate from a country with a reliable drug regulatory authority shall suffice
as determine by BFAD.
3.1.16 Duly authenticated government certificate attesting to the registration
status of the manufacturer
This Certificate shall be issued by the regulatory agency on pharmaceuticals
from the drug products country of origin. It shall contain a statement that the
manufacturer is duly registered with the regulatory agency, and that the
manufacturing facilities are regularly inspected and are found to conform with
current Good Manufacturing Practices (GMP)
(Note: Certifications issued by the competent authority of the exporting
country in accordance with the WHO Certification Scheme on the Quality of
Pharmaceutical Products moving in International Commerce are highly
acceptable.)
3.1.17 Bioavailability/Bioequivalence Studies for products under List B (As

per Bureau Circular No. 01 s. 1997)
Bioavailability studies are conducted to determine the rate and extent to
which the active drug ingredient is absorbed from a drug product and
becomes available at the site(s) of action. It is a crucial determinant in the
rational formulation of dosage forms and influences the manner and route of
drug administration.
Bioequivalence utilizes the concept of bioavailability in assessing the
comparability of drug products containing the same amount of active
ingredients but produced at different time or by different manufacturers.
Bioavailability and bioequivalence studies are an important component of
drug regulation and control to ensure that only products of good quality are
allowed in the market for consumption. (Refer to Annex REQUIREMENTS
FOR THE SUBMISSION OF BIOAVAILABILITY/BIOEQUIVALENCE
STUDIES)
3.2
NEWLY INTRODUCED DRUG

3.2.1
Application for Initial Registration shall comply

requirements under Established Drugs as follows:
with
all
the
1. Application Letter
2. Certificate of Brand Name Clearance
3. Certificate of Agreement between Manufacturer and Trader or DistributorImporter/Exporter
4. Unit dose and batch formulation
5. Technical/Quality specifications of all raw materials
6. Certificate of Analysis of active ingredient
7. Technical/ Quality specifications of finished product
8. Certificate of Analysis of finished product
9. Full description of the methods used, the facilities and controls in the
manufacture, processing and packaging of the finished product
10. Details of the assay and other test procedures for the finished product
11. Detailed report of stability studies to justify claimed shelf-life
12. Labels or specimen of the proposed label and other labeling materials
such as inserts, brochures, etc.
13. Samples in market or commercial presentation
14. Duly authenticated Certificate of Free Sale from the country of origin
15. Duly authenticated government certificate attesting to the registration
status of the manufacturer
3.2.2
Certificate of the Medical Director registered with BFAD

To facilitate the objective evaluation of drugs, to provide adequate
information to the consuming public, and to ensure safety and efficacy of
drugs, all establishments engaged in the manufacture and distribution of
drugs must have a Medical Director who is a registered physician with
knowledge and training in basic and clinical pharmacology.
All communications with the BFAD regarding New Drugs and Investigational
New Drugs and matters arising from clinical investigation shall be coursed
through the Medical Director.
All labeling materials including inserts, brochures and other
labeling/promotion materials must be approved by the Medical Director.
3.2.3
Reference Standard and its corresponding Certificate of Analysis

A sufficient amount of reference standard shall be submitted to enable the
BFAD to test the purity or potency of the drug product.
Reference Standards are specifically required in many Pharmacopoeial
assays and tests where results are determined on the basis of comparisons
of the specimen under test with a Reference Standard that has been freed
from or corrected for volatile residues or water content.
An analytical report providing the results of the test carried out to establish
the identity, purity and potency of the reference standard shall also be
submitted.
3.2.4
Pre-clinical Data
Before initial human studies are permitted, the full spectrum of pharmacologic
properties of the new drug must be extensively investigated in animals.
Animal researches, are done to provide evidence that the drug has sufficient
efficacy and safety to warrant testing in man.
Pre-clinical studies shall include pharmacodynamics, pharmacokinetics, and
toxicity studies of the drug.
1. Pharmacodynamics
Pharmacodynamic studies are done for the following purposes:
1. to identify the primary action of the drug as distinguished from the
description of its resultant effects.
2. to delineate the details of the chemical interaction between drug and
cell or specific receptor site(s), and
3. to characterize the full sequence of drug action and effects.
a. Pharmacologic effects - properties relevant to the proposed
indication and other effects.
Pharmacodynamic data shall demonstate the primary
pharmacologic effect of the drug leading to its development for
the intended use(s) or indication(s). it shall also show the
particular tissue(s)/organ(s) affected by the drug and any other
effect it produces on the various systems of the body.
b. Mechanism of action including structure-activity relationship
(SAR)
Pharmacodynamic data shall also demonstrate the correlation of
the actions and effects of drugs with their chemical structures.
Structure-activity relationship is an integral link in the analysis of
drug actions since it is well known that the affinity of a drug for a
specific macromolecular component of the cell and its intrinsic
activity are intimately related to its chemical structure.
2. Pharmacokinetics
Pharmacokinetic data form the basis for prediction of therapeutic doses
and suitable dosage regimen.
These date shall demonstrate the following:
1. the rate and extent of absorption of the drug using the intended route
of administration;
2. the distribution patter including a determination of the tissues or
organs where the drug and its metabolites are concentrated
immediately after administration and the time course of their loss
from this sites;
3. the metabolic pathway of the drug or its biotransformation and the
biological activity of the metabolites;
4. the route of excretion of the drug and its principal metabolites and the
amount of unchanged substance and metabolites for each route of
excretion;
5. the drugs half-life or the rate that it is eliminated from the blood,
plasma or serum.
3. Toxicity data
Toxicity date shall include results of acute toxicity, subchronic and
chronic studies done on different species of animals.
1. Acute Toxicity
Acute toxicity data shall show the median lethal dose of a drug.
Ideally, the study shall be carried out in at least two (2) species of
animals, one (1) rodent and the other non-rodent, using 5 dose levels
with the appropriate number of test animals. Example: 10 rodents per
dose level with the drug given as a single dose and the animal
observed for seven (7) days or more (preferably 14 days). The route
of administration should that be anticipated for use in man, i.e., oral
(by gavage) if to be administered orally.
Acute toxicity data should be able to:

1.
2.
3.
4.
define the intrinsic toxicity of the drug

assess susceptible animal species
identify target organs
provide information on risk assessment after exposure to the
drug
5. provide information for the design and selection of dose levels for
future chronic studies
The following parameters should be established:
1.
2.
3.
4.
5.
Lethal dose 50 (LD50)

Effective dose 50 (ED50)
Therapeutic index
No observable adverse effect level (NOEL)
Toxidrome
2. Subchronic Toxicity
Subchronic toxicity studies are carried out using repeated daily
exposure to the drug over a period of 21-90 days with the purpose of
studying the toxic effects on target organs, the reversibility of the
effects and the relationship of blood and tissue levels on the test
animals.
The following should be contained in the subchronic toxicity data:
1. a determination of the adverse effects from repeated exposures
to a chemical over a portion not exceeding 10% of the average
life span.
2. A determination of the cumulative toxicity and the development of
tolerance in target organ with continuous exposure.
3. A monitored hematologic, renal, hepatic and biochemical
changes.
4. A determination of the maximum tolerated dose or the dose with
no observed effects in animals.
The parameters used for objective evaluation of drug effects in animals
are as follows:
1. Physiologic changes such as body weight, food and water
consumption, grooming, bowel movement and urination,
temperature, heart rate and respiratory rate.
2. Hematologic such as Hemoglobin (Hb), Hematocrit (ct), White
Blood Clot (WBC), Differential count, platelet and reticulocyte
count
3. Biochemical such as liver enzymes, alkaline phosphatase, total
protein, albumin, globulin, BUN, creatinine, blood sugar, uric acid
and cholesterol.
4. Urinalysis
5. Neurological
6. Behavioral
7. Post-mortem analysis (anatomical and histopathological)
8. No observable effect level
3. Chronic Toxicity
Chronic toxicity studies constitute important steps in the analysis of a
chemical. The entire lifetime exposure of an individual or animal to
the environment or chemical is an on-going process which neither
acute nor subchronic toxicity study can provide. The effect on
animals when small doses of the drug are given over a long period of
time may not be the same as when large doses are given over a
short period.
Chronic toxicity studies are done to determine the no observed
adverse effect level (NOEL) and to set the acceptable daily intake
(ADI) tolerance and threshold limits. The parameters to be observed
are the same as in subchronic studies.
4. Special Toxicity Data
Special toxicity studies in animals are conducted to
1. determine the safety of the drug or its preparation through acute,
sub-acute and allerginicity tests using appropriate species of
animals.
2. Evaluate the effects of the drug on reproduction when given

prenatally using fertility and gestation rate as parameters and the
effects on the fetuses when given to the lactating dams
3. Determine the morphological and functional effects on the fetus
when the drug is administered to the pregnant animal during the
period of organ development (organogenesis)
4. Evaluate the mutagenicity potential of the drug
5. Determine the potential of the drug to induce tumor or cancer
formation with prolonged administration.
Reproduction tests are designed to evaluate the effect of the
drug on the general reproductive performance of animals starting
at implantation and continuing through the weaning period in
doses significantly greater than those intended for man or in
doses that give significantly higher blood and/or other tissue
concentrations than those achieved in man.
Since test substances may adversely affect reproductive
processes in several ways, at least three (3) tests are required
for most new drugs:
1. Multigeneration reproduction study provides information on
the fertility and pregnancy in parent animals and subsequent
generations. The effects of a potentially toxic substance
could be determined by the reproductive performance
through successive generations such as adverse effects on
the formation of gametes and on fertilization and to detect
gross genetic mutations which may lead to fetal death, fetal
abnormalities or inadequate development or abnormal
reproductive capacity in the F1 generation. This study can
also reveal, adverse drug effects that occur during pregnancy
or during lactation.
2. Teratologic study determines the effect of a chemical on the
embryonic and fetal viability and development when
administered to the pregnant female rodent (rat) or nonrodent (beagle dog or monkey) during the period of
organogenesis. The specific objectives include: (a)
characterization of the type and incidence of malformations
in comparison with negative and positive controls through
detailed skeletal and visceral organ examination (Wilson
Cutting Technique) (b) calculation of pregnancy rate,
implantation efficiency, and fetal vialibility, and (c) evaluation
of the effect of treatment of chemical on maternal weight,
mortality, behavior, and fetal weight, including male/female
ratio.
3. Peri-natal and post-natal study determines the effects of
drugs or chemical given to the pregnant animal in the final
one-third of gestation and continued throughout lactation to
weaning of pups. The study should give data on the
following:
(a) Labor, as to presence of dystocia, duration of labor,
onset of labor.
(b) Getation as to duration and weight gain of dams during
pregnancy
(c) Litter as to number of pups (litter size), weight of pups,

nursing behavior of pups, physiologic and anatomic
parameters (food and water consumption, length, etc.)
and effect of crossover nursing of pups.
A concurrent negative control of animal must be run
together with the treated groups (at least 3 dose levels).
2. Carcinogenicity
Carcinogenicity tests in animals are required when the drug is likely
to be given to humans continuously or in frequent short course
periods to determine whether chronic administration can cause
tumors in animals. Mice and rats are the rodents of choice while dogs
or monkeys are preferred non-rodents. These tests may be designed
to be incorporated in the protocol for chronic toxicity studies wherein
the animals are exposed to the drug after weaning and continued for
a minimum of two years. At least 3 dose levels are used with the
highest dose approximating the maximal tolerated dose and the route
should be similar to that anticipated in man. Repeated expert
observation, palpation and thorough examinations of animals for any
lumps or masses are essential. All animals must be thoroughly
autopsied and histological examination of all organs should be
carried out.
For drugs which are related to known carcinogens, in vivo bioassay
may be used such as skin neoplasm induction in mice, pulmonary
neoplasm induction in mice, breast cancer induction in female
Sprague-Dawley rats and altered foci induction in rodent liver.
The use of negative and positive controls allow for a statistical
comparison of the incidence of tumors in the test groups.
3. Mutagenicity
Mutagenicity tests have the primary objective of determining whether
a chemical has the potential to cause genetic damage in humans.
Animal model systems, both mammalian and non-mammalian
together with microbial systems which may approximate human
susceptibility, are used in these tests. In most recommended tests,
three categories of genetic damages are investigated: Chromosome
mutations, point mutations and primary DNA damage by in vivo and
in vitro assay.
3.2.5 Clinical Data
Data from clinical trials are the basis in designing the most appropriate
treatment of future patients with a given medical condition.
The following documents shall be included in the submission of clinical data:
1. Certification of an independent institution review board of approval of
clinical protocol and monitoring of clinical trial.
An independent Institutional Review Board (IRB) shall be responsible for
the initial and continuing review and approval of the clinical investigation.
An approval of the clinical protocol by the IRB shall be obtained before
any stage of the clinical trial is started. All changes in the research
activity and all unanticipated problems involving risks to human subjects
should be promptly reported by the clinical investigation(s) to the IRB.
2. Clinical Investigation Data

1. Phase I Clinical Drug Trial
Phase I Clinical Drug Trial consists of initial testing of the study drug
in humans, usually in normal volunteers but occasionally in actual
patients. The number of subjects is small (N= 15 to 3). SAFETY
evaluations are the primary objectives and attempt is made to
establish the approximate levels of patient tolerance for acute and
multiple dosing. Basic data on rates of absorption, degree of toxicity
to organs (heart, kidney, liver, hamatopoietic, muscular, nervous,
vascular) and other tissue, metabolism data, drug concentrations in
serum or blood and excretion patterns are also obtained. Subjects
shall be carefully screened. Careful monitoring for adverse or
untoward effects and intensive clinical laboratory tests are required.
This study shall be conducted by an approved or accredited Clinical
Pharmacologist. A written informed consent of subject is necessary.
2. Phase II Clinical Drug Trial
Phase I Clinical Drug Trials are initial studies designed to evaluate
EFFICACY of the study drug in a small number of selected
populations or patient for whom the drug is intended which may be
open label or single or double blind. Blood levels at various intervals,
adverse experiences, and additional Phase I data may be obtained.
Small doses are gradually increased until the minimal effective dose
is found. All reactions of the subjects are carefully recorded.
Preliminary estimates of the dosage, efficacy and safety in man are
made.
The second part of Phase II consists of pivotal well controlled studied
that usually represent the most rigorous demonstrations of a drug
efficacy. Relative safety information is also determined in Phase II
studies. A larger number of patients are enrolled into the second part
(N= 60 to 200 subjects).
Phase II studies are conducted by accredited Clinical
Pharmacologists. Phase II second part studies may be conducted by
well qualified practitioners or clinicians who are familiar with the
conditions to be treated, the drug used in these conditions to be
treated, the drug used in these conditions and the methods of their
evaluation. A written informed consent of patients-participants is
needed.
Phase II clinical Trial is usually carried out in a hospital for more
careful supervision and control.
3. Phase III Clinical Drug Trial
Phase III clinical drug trials are studies conducted in patient
populations for which the drug is eventually intended.
These studies generate data on both safety and efficacy in relatively
large numbers of patients under normal use conditions in both
controlled and uncontrolled studies. The number of patients required
vary (1,000 to 10,000). These studies provide much of the
information that is needed for the package insert and labelling of the
drug.
This phase may be conducted as a multicentric trial among
accredited clinicians. The informed consent of participating subject is
preferably in written form.
4. Biovailability
Bioavailability studies are conducted to determine the rate and extent
to which the active substance or therapeutic moiety is absorbed from
a pharmaceutical form and becomes available at the site of action.
3. Name(s) of investigator(s) and their curriculum vitae
The name(s) and address(es) of the investigator(s) and
subinvestigation(s) (e.g. research fellows, resident physicians) who will
be assisting the investigator(s) in the conduct of the investigation should
be submitted.
A curriculum vitae or other statement of qualifications of the
investigator(s) showing the education, training and experience that
qualifies the investigator as an expert in the clinical investigation of a
drug should also be submitted.
The investigator shall be well qualified by
experience to conduct investigational studies of
is affiliated with a recognized medical school
institution recognized for its excellence or is
qualified.
scientific training and

the subject drug and he
or with an independent
otherwise appropriately
The training and experience needed will vary, depending upon the kind of
drug and the nature of the investigation. In Phase I, the investigator must
be able to evaluate human toxicology and pharmacology. In Phase II, the
clinicians should be familiar with the conditions to be treated the drugs
used in these conditions and the methods of their evaluation. In Phase III,
in addition to experienced clinical investigators, physicians not regarded
as specialists in any particular field of medicine may serve as
investigators, properly guided by a competent clinical investigator who
will collate all the data and be responsible for the final result of the body.
At this stage a large number of patients may be treated by different
physicians so that a broad background of experience may be secured.
4. Name(s) of center/institution wherein the clinical investigation was
undertaken
The institution/center must be accredited by the regulatory agency and
must have an independent ethical and technical review boards. The
facilities and laboratories must meet the requirements for the phase of
clinical trial that will be undertaken in such institution/center.
Phase I clinical trials require facilities and human resource capabilities of
the highest degree. These requirements are usually met only by
institutions/center in well developed countries. Phase II and III may be
undertaken in academic institutions and tertiary hospitals with trained
clinical pharmacologists, specialists and paramedical personnel.
The capabilities and standard of these institutions/centers must have
been certified by the appropriate government agency as meeting the high
standard of Good Laboratory Practice (GLP) and Good Clinical Practice
(GCP)
The Medical Director of such institution/center or hospital must certify that
such clinical trial is being allowed to be conducted in such institution or
hospital.
5. Protocol for Local Clinical Trial
Local clinical trials are conducted to determine the safety, efficacy and
suitability of the recommended dosage and therapeutic dose regimen to
the local patient population. These trials can only be conducted after the
protocol for a local clinical trial is approved by an accredited independent
institutional review board and a temporary permit to market the drug
locally is granted.
The protocol for the local trial shall include the following:
1. Study Title
2. Names of Investigator(s) including supervising investigator, principal
investigator, co-investigator(s).
3. Funding/Sponsoring Agency
4. Summary of the Proposed Study
5. Introduction including an identification of what is being studied, an
explanation of why the study is valid or the scientific rationale.
6. Objective(s) of the study indicating the general objective and specific
objective(s).
7. Study Design e.g. descriptive study, case control, cohort, randomized
concurrent trial.
8. Methods including a description of the study subjects, sample size,
description of the study procedure, and a description of outcome
measurements.
9. Data analysis including the criteria for substantive and statistical
success, definition of drop-outs, withdrawals, treatment failure,
details of statistical strategy to be used, and a specification of data
handling, collation and computer use.
10. Ethical Consideration including
a. Good outweighing harm
b. Free informed consent
c. Freedom to withdraw from the study at any time
d. Confidentiality
11. Indemnification Policy which is compensation statement indicating
availability payment for treatment or free treatment hospitalization in
case of an adverse drug experience.
12. Time schedule or duration of clinical trial.
13. Duties and responsibilities of research personnel.
a. The investigator must conduct the studies in conformance with
the Declaration of Helsinki or the laws and regulations of the
country in which the research is conducted, whichever represent
the greater protection of the individual.
b. The investigator must keep careful records of his study and
retain them for at least two years after the new drug application is
approved. The records must be available promptly to the drug
sponsor (usually the drug manufacturer) and to the drug
regulatory agency. Progress reports must be sent to the sponsor
at intervals not exceeding one year.
c. The investigator must send emergency reports to the sponsor
and the regulatory agency when dangerous adverse effects are
observed.
d. The investigators must observe the regulations regarding

consent of human subjects being given an investigational drug.
14. Bibliography
15. List of Hospital Resources/Personnel Required.
16. List of Basic Sciences Resources
17. Appendices including informed consent form, patient/case report
form, flowchart of activities, questionnaire, dummy tables and graphs.
18. A statement that the protocol was reviewed and approved by the
Research Committee and the Director (and Dean, if applicable) of the
institution/hospital.
3.3 PRODUCTS WITH
ADMINISTRATION
3.3.1
NEW
INDICATION(S)
OR
NEW
ROUTE
OF
Application for Initial Registration shall comply with the following

requirements under Established Drug
1. Application letter
3. Technical specifications of all raw materials
4. Certificate of Analysis of active raw material
5. Technical specification of finished product
6. Certificate of Analyses of finished product
manufacture, processing and packaging of the product
8. Details of the assay and other test procedures for finished product
including data analysis.
10. Sufficient samples in market or commercial presentation for
laboratory analysis and representative sample for PSD.
3.3.2
Pharmacokinetic data
Pharmacokinetic studies should be conducted to determine the most
suitable dosage regimen for the new indication or the new route of
administration.
It is important to conduct pharmacokinetic studies relating to the new
route of administration since the metabolic pathways of a drug substance
and the biological activity of its metabolites may vary depending on the
route it is administered.
3.3.3
Phase III clinical trial for the new indication(s) or the new route of
administration
Phase III clinical studies should be aimed at determining the safety and
efficacy or the drug product for its new indication or new route of
administration.
For studies on a new indication, Phase III clinical trial should be
conducted in patient population for which the new indication is intended.
3.3.4
Local Clinical Trial (optional)
Local clinical trials are conducted to determine the safety, efficacy and
the most appropriate dosage or dosage regimen for the new indication in
local patient population.
3.4 PRODUCTS WITH ADDITIONAL DOSAGE OR DOSAGE STRENGTH
3.4.1

5. Technical specifications of finished product
6. Certificate of Analyses of finished product
laboratory analysis and representative sample for PSD
3.4.2
Pre-clinical studies
1. Toxicology data for increased dosage to ensure that the addition in
the amount of active ingredient will not diminish the desirable effects
of the drug.
3.4.3
Phase III Clinical Drug Trial (optional)
3.4.4
Local Clinical Trial (optional)
3.5 PRODUCTS WITH NEW DOSAGE FORM

3.5.1


laboratory analysis and representative sample for PSD
11. Unattached generic labeling materials: label, box, insert, blister/foil
strip
12. Requirements for sterile products
3.5.2
Bioavailability or Bioequivalence Data, as needed

Bioavailability is largely dependent in the ability of the drug product to
release the active ingredient at the site where it is intended to be
absorbed.
Problems on bioavailability are more especially defined in solid oral
dosage forms of drugs. medically significant cases of bioinequivalence
rest mainly on four causal factors: particle size of an active ingredient;
magnesium stearate in excess as a lubricant-glidant; coatings especially
shellac; inadequate disintegrant. Every one of the factors is reactive to
dissolution testing.
3.6 PRODUCTS WITH CHANGE IN:

1. Application for Initial Registration shall
requirements under Established Drugs
comply
with
the
following
a)
b)
c)
d)
e)
f)
g)
Application letter
Copy of latest Certificate of Product Registration
Certificate of Analysis of active raw material
Technical specifications of finished product
Certificate of Analysis of finished product
Details of the assay and other test procedures for finished product
h) Detailed report of stability studies to justify claimed shelf-life
i) Sufficient samples in market or commercial presentation for laboratory
analysis and representative sample for PSD
j) Actual unattached generic labeling materials; label, box, insert, blister/foil
strip
k) Requirements for sterile products
2. Notification of the change in formulation including a justification for such
change.
3. Bioavailability of Bioequivalence data, as needed.
3.7 PRODUCTS FOR MONITORED RELEASE PRIOR TO APPROVAL FOR
GENERAL USE
Newly Introduced Drugs (NID) (with history of 5 years registered use 5000 patient
exposure in other countries), will be required to complete clinical pharmacological
studies and pass through a 3-year Initial Registration (Monitored Release) before
becoming eligible for application and approval for General Use.
The model protocol for monitored release is as follows:
An Uncontrolled Clinical Study reported the therapeutic effects and adverse
reaction for 1000 patients per year or 3000 patients over 3 years, provided
however that if the drug product is for a very limited therapeutic indication the
1000 patients/year requirement will be waived and only 10% of total patients is
given the drug will be required to be monitored and reported to BFAD by the
Pharmaceutical Company.
3.8 PHASE IV CLINICAL TRIAL FOR PRODUCTS UNDER THE FOLLOWING

CATEGORIES:
1. NEWLY INTRODUCED DRUG
2. ESTABLISHED DRUG WITH
a. NEW INDICATION OR NEW ROUTE OF ADMINISTRATION
b. ADDITIONAL DOSAGE OR DOSAGE STRENGTH
Phase IV clinical drug trials are conducted after the drug is marketed to provided
additional details on the drugs efficacy and/or safety profile.
The first part is done through a monitored release of drug to selected medical
centers and qualified physicians. Monitoring of drugs safety and efficacy is done
and impact under limited marketing is obtained (See Sections 3.7 for details)
Further, Postmarketing surveillance (Part II of Phase IV) is the evaluation of the
drugs efficacy and safety among patients under conditions of general drug use.
These are primarily observational or non-experimental in nature. Patterns of drug
utilization are studied. All physicians agreeing to participate in organized reporting
may conduct this phase of the study.
Adverse drug experiences shall be monitored and an independent review board
shall evaluate the reports to determine cause-effect relationship or to conclude
whether an adverse drug reaction has occurred or not.
4. RENEWAL REGISTRATION
Renewal of registration of all drug products is necessary to enable the authorities to
check the quality, safety and effective dose regimen of drug products currently available
to the public. Problems of drug interaction in vitro and in vivo must be assessed during
renewal of registration. Any change in precautions, cautions and warnings shall be
implemented during renewal of registration, if not done earlier.
4.1 Application for Renewal Registration shall comply with the requirements under
Established Drug as follows:
1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
11.
Application letter
Copy of latest Certificate of Product Registration
Detailed report of stability studies to justify claimed shelf-life (3 batches)
Sufficient samples in market/commercial presentation for laboratory
Actual unattached generic labeling materials; label, box, insert, blister/foil
strip
Requirements for sterile products
4.2 Application for renewal registration of drug or pharmaceutical specialty shall be

file within three (3) months before the expiration date of the Certificate of Product
Registration.
4.2.1
4.2.2
A surcharge of 50% or renewal registration fees shall be imposed

upon application for renewal registration filed within three (3)
months after expiration date of CPR.
Application for renewal registration filed three (3) months after
CPRs expiration date shall be considered as initial registration.
4.3 Payment of surcharge shall not make the product under the renewal process
eligible for conditional registration.
5. FIXED-DOSE COMBINATION DRUG PRODUCTS
Definition:
Fixed Dose Combination Drug Products (FDCs) are pharmaceutical preparations
containing two or more pharmacologically-active ingredients in a single formulation or
dosage form.
Scope of these Guidelines: (A.O. 96 series 1990)
All products classified as FDCs are covered by these guidelines. These are three
categories of products included:
5.1 Currently registered products already recognized and identified by BFAD as FDCs.
5.2 Currently registered product which may later be classified as FDCs
5.3 Products with pending or for future initial registration under the category of FDCs.
All these categories of FDCs are covered but the specific applicability will be defined
below.
Safety, Efficacy and Quality Criteria
The drug regulatory criteria of safety, efficacy and quality shall be applied to the specific
class of FDCs using the following rules:
1. The FDC drug product must comply with the appropriate requirements of A.O. 67 s.
1989 on registration of drug products.
2. The drug establishment seeking to register the FDC drug products should comply
with the appropriate requirements of A.O. 56 s. 1989 on the registrations of drug
establishments.
3. In addition to the above, the FDC drug product in its final dosage form must be
proven to adhere to all the following criteria:
(a)
(b)
(c)
(d)
The active and inactive ingredients should be pharmaceutically (i.e. chemically,

physically) and pharmacologically compatible in combination.
The FDC taken as a whole should have clinical and therapeutic advantage over
the individual active ingredients taken separately. In this respect, acceptable
clinical and therapeutic advantage involves more than additive affect,
convenience or better compliance. It should include each advantages as
complementary or synergistic pharmacological action or therapeutic effect, or
reduction in adverse drug reaction.
It must not contain any ingredient whose proper administration or clinical use
require special adjustments different from or in conflict with its other ingredients.
It must not contain active ingredients with abuse potential (those identified in List
A of A.O. 63 s. 1989), with a narrow margin of safety and/or requires special
precautions in its use and/or with bioequivalence problems (those identified in
List B of A.O. 63 s. 1989), and which are banned or not yet registered in the
Philippines.
Currently registered FDC drug products are classified into use groups and order
of priority for review. The classification is based on PNDF characterization of
products active ingredients and the manufacturers claims of the nature of the
drug action in its approved product.
PRIORITY I
PRIORITY III
1. Anti-infectives
2. Anti-asthmatics
3. Cough/Cold remedies
1. Gastro-intestinal preparations
2. OB/Gyne preparations
3. Musculoskeletal preparations
4. Urinary tract preparations
5. Vitamins-minerals
6. Eye-Ear preparations
7. Dermatologicals
8. Dermatologicals
9. Others
PRIORITY II
1. Anti-TB
2. Cardio-vascular preparations
3. Endocrine/metabolics
4. Drugs acting on central nervous
System
5.4 Fixed Dose Combination Drug Products listed in the latest edition of the
Philippine National Drug Formulary and complying with A.O. 67 s. 1989 shall be
accepted for registration without satisfying the requirements stated in Section
4.2 of A.O. 96 s. 1990.
6. PRODUCTS WITH CHANGE OF MANUFACTURER (M.C. No. 12 s 1991)
6.1 When a drug establishment changes manufacturer for its product(s) to one that has
better technical capabilities as evidenced by a record showing no deficiencies or only
minor deficiency (not substantively affecting product quality) in either GMP or its
whole product lines, a conditional certificate of product registration (CPR) may be
granted following the registration procedure defined under BFAD Circular No. 12 s.
1991.
6.2 Compliance with the following requirements under Established Drug as follows:
1.
2.
3.
4.
5.
6.
7.
Application letter
Original Certificate of Product Registration
8. Sufficient samples in market/commercial presentation for laboratory
9. Actual unattached generic labeling materials; label, box, insert,
blister/foil strip
6.3 The conditional CPR shall be effective for a period of one (1) year subject to the
results of the BFD Laboratory tests and stability studies for the product conducted by
the new manufacturer.
7. PRODUCTS WITH IMPROVEMENT OF IMMEDIATE CONTAINER OR PACKAGING
(M.C. No. 16 s1991)
7.1 Encouraging technical improvement of validly registered drug products, a conditional
initial registration may be granted to products whose only change is an improvement
in the immediate container or packaging. For this purpose, the procedure under the
Memorandum Circular No. 16 s. 1991 shall be observed.
7.2 Compliance with the following requirements under Established Drug
2. Copy of latest Certificate of Product Registration
8. Sufficient samples in market/commercial presentation for laboratory
9. Actual unattached generic labeling materials; label, box, insert,
blister/foil strip
7.3 If the establishment opts to retain the registered products with the old packaging
specifications, a new registration number will be assigned to the same product with
the new packaging specifications; however if the establishment applies to use the
same DR number of the old product for the new, the product with the old packaging
specifications shall be considered automatically phased out after the Conditional
CPR for the new product is approved. In this case, the original CPR with the old
packaging specification shall be submitted.
7.4 The Conditional CPR shall be valid for a period of one (1) year from the date of
issue. It shall be subject to the satisfactory result of laboratory tests and of stability
studies.
8. REGISTRATION OF BRANDED VERSION OF REGISTERED UNBRANDED GENERIC
DRUG PRODUCT AND GENERIC VERSION OF REGISTERED BRANDED DRUG
PRODUCT (AS PER M.C. No. 10-A S 1992)
8.1 Requirements for Branded version
A manufacturer, trader or distributor-Importer who has a registered unbranded
generic drug product may apply for registration of the branded version of the said
product provided that if the registration of that generic product was processed through
the Special Lane (M.C. No. 5 s. 1990) under product category B, the registration of
the branded version will become effective only one (1) year from the date of
application for the branded version but not less than one (1) year after the date the
generic version was approved. (Product category B under MC No. 5 s. 1990 is a
special privilege for generic (unbranded) drug product, hence this rule).
The applicant shall submit together with his application the following:
a) A copy of the Certificate of Brand Name Clearance
b) If the company opts to retain the unbranded version, a copy of the Certificate of
Product Registration of the generic drug product, if the company will no longer
market the generic version, the current original Certificate of Product Registration.
c) A prototype of the proposed complete commercial form and presentation of the
branded version of the product including labels and inserts.
d) Unit dose and Batch Formulation
e) Technical/Quality Specification of the finished product
8.2 Requirements for Generic version
A manufacturer, trader or distributor-importer who has a registered branded drug
product, may apply for registration of the unbranded generic version of the same.
The applicant shall submit together with his application the following:
a) If the company opts to retain the branded version a copy of the Certificate of
Product Registration of the branded version; if the company will no longer market
the branded version, the current original Certificate of Product Registration.
b) A prototype of the proposed complete commercial forms and presentation of the
unbranded generic version of the product.
c) Unit dose and batch formulation
d) Technical/Quality specifications of finished product
9. The foregoing guidelines shall not preclude the BFAD form requiring any specific
technical data whenever question of safety, efficacy and quality arises during the
evaluation.
These 1997 Guidelines shall be amended or modified after consultation with the
pharmaceutical sectors to update the same with technological advancement in
pharmaceutical products.
(Sgd) QUINTIN L. KINTANAR, M.D., Ph. D., CESO l

Director
Date approved:
January 30, 1997
Date of Effectivity
April 1, 1997
GUIDELINES ON THE STABILITY TESTING OF PHARMACEUTICALS

Table of Contents
Preamble
1. General Principles
2. Stability Trial Design
2.1 Active raw material
2.2 Finished Product
3. Appropriate Tests
3.1
3.2
3.3
3.4
3.5
3.6
3.7
4.
5.
6.
7.
8.
General
Assay
Degradation products
Physical products
Preservative efficacy
Dissolution rate
High humidity studies
Presentation of Results
Prediction of Shelf-Life from Stability Data
Product Modifications
Prospective Extensions of Shelf-Life for Individual Batches
Shelf-life Extensions According to an Approved Protocol
Appendices
1. Acceptable Temperature Storage Conditions Which May Appear on Labels
2. Common Deficiencies in Stability Data and Trial Design
3. Glossary of Terms
Preamble
These notes provide guidance as to the design, conduct and reporting of stability studies. These
guidelines primarily cover:
-
products containing drugs which are prepared by chemical synthesis

products containing drugs which are pure chemical entities isolated from a natural source,
e.g. vincristine, digoxin
radiopharmaceuticals (but see below)
products containing drugs which are produced by microbial fermentation, principally
antibiotics and some anticancer drugs.
materials of biological origin (see below)
Materials of biological origin. The principles described in this document also generally apply to stability
studies on materials of biological origin, such as hormones, allergens, modified animal tissues,
vaccines and the products of genetic engineering or other newer biological techniques. However
some specific guidelines may not be appropriate for biologicals, in particular:
References to chemical assay techniques, such as the preference stated in 3.3 for
chromatographic methods for decomposition products, may not always be appropriate for
biologicals.
It may not always be possible to establish degradation pathways and identify
decomposition products formed in significant amounts (see 2.1 and 3.3)
The degradation of biologicals is not usually amenable to kinetic analysis and
extrapolation from accelerated testing (see 5)
Stability data for biologicals will be evaluated on a case by case basis, having regard to the nature of
the product and the methods of analysis (physical, chemical biological) which are appropriate for that
product.
I. General Principles
The objectives of a stability study is to determine the period of time during which a pharmaceutical
product meets appropriate standards when stored under defined conditions. As a minimum, the
product must be shown to comply with relevant specifications for the whole of its shelf-life.
The following statement, which appears in the 1993 edition of the British Pharmacopoeia, reflects a
principle which should be familiar to any pharmaceutical manufacturer:
A manufacturer must recognize that a product or material may be challenged at any time during its
claimed period of use by the methods of the Pharmacopoeia and that it must then comply with the
pharmacopoeia requirements. These requirements allow for acceptable levels of change that may
occur during storage and distribution and reject articles showing unacceptable levels of change.
Frequently a manufacturer will need to apply more stringent test limits at the time of release of a batch
of the product or material in order to ensure compliance. (BP 1993, p xxii)
Thus the difference between release and expire specifications must take into account the results of
stability testing.
The maximum permitted shelf life is normally five years.
2. Stability Trial Design
2.1 Active raw material. An assessment of the stability of the active raw material (see Glossary of
Terms) is required for new drugs and is useful in support of shelf lives for new formulations of
existing drugs. such information provides a useful guide to the problems which may be
encountered during stability studies on finished products.
Studies should establish the inherent stability characteristics of the molecule, in particular the
degradation pathways, the identity of degradation products formed in significant amounts and
the suitability of proposed analytical procedures for quantitation of both the drug substance
and degradation products. The nature of the studies will depend on the drug substance but is
likely to include the effect of elevated temperature, susceptibility to moisture and oxidation,
and the effect of light. The effect of pH may be important when the finished product is an
aqueous solution or suspension, in the latter case by means of effects on the fraction of drug
actually dissolved, however small.
The kinetics of degradation of the active raw material cannot be assumed to apply to
reactions which occur in the finished product, and care should be exercised in extrapolating
on the basis of such data.
2.2 Finished product
2.2.1
The formulation must be the same as that proposed for registration in the
Philippines. Stability data on related formulations may be submitted as supporting
evidence provided the differences between the formulation employed in the stability
trial and that proposed for registration are clearly stated. A shelf life will not normally
be allocated for the purposes of registration if there are no data on the formulation to
be registered.
All manufacturing processes must have been carried out on the batches used in the
stability trial, e.g. filtration, packaging, sterilization.
2.2.2.
The product should be tested in the container/closure system in which it will be

registered in the Philippines. If the product is to be registered in more than one
container/closure system, stability data should normally be provided for each
presentation (however see 6.2 below). Stability data in other types of pack are of
limited value, unless comparative studies of the two types of pack are provided which
clearly demonstrate the equivalence or superiority of the container/closure intended
for registration over the system used on the stability trials.
2.2.3.
Stability information should be generated on a minimum of three batches. Where this

information has been obtained on pilot production batches. A full trial must be
conducted using at least three production batches as soon as they become available.
Where the product is registered in several strengths, stability data should be
generated on three batches of each strength, unless the different strengths are direct
scales (see Glossary of terms) in which case at least one batch of each of the highest
and lowest strengths should be tested. For multiple strengths where the highest and
lowest strengths bracket the others in terms of proportions of excipients, only the
highest and lowest strengths normally need to be tested (two batches of each)
2.2.4.
Conditions of storage likely to be encountered in the Philippines should be considered

in designing the stability trial. Storage conditions should be clearly defined, preferably
in terms of the categories specified in Appendix 1. Lighting conditions should be
specified.
The use of uncontrolled temperature conditions in stability trials is unacceptable.
Terms such as room temperature and normal warehouse conditions are
discouraged as these allow the product to be exposed to a wide range of conditions
and make shelf life assessment difficult. Where a shelf life is based upon uncontrolled
storage conditions, it will usually be shorter than the duration of the submitted study.
If storage in a refrigerator is proposed without the caution Do not freeze, then
stability, particularly physical stability (e.g. no formation of a precipitate, no
denaturation of a protein) at about -50C must be demonstrated.
Stability studies at elevated temperatures are useful in predicting longer term shelf life
periods from short term data (see part 5 below) but these predictions should be
verified by studies on production batches in the pack intended for registration at the
maximum recommended storage temperature for the full term proposed, for example
0
at 30 C, if the recommendation storage temperature statement is Storage below
0
30 C
2.2.5.
The cycling effect of night and day temperatures and humidity can be important for
example where the drug is present partly in suspension and partly in solution. Cycling
conditions may be simulated in environmental cabinets. The data are useful in
confirming the stability of the product under conditions of stress. However at is
difficult to derive accurate predictions for the shelf life of a product from this
information and it is not a formal requirement.
2.2.6.
Where the product is to be registered in a moisture permeable material such as

polyvinyl chloride (PVC) or some grades of polyehtylene, or where the closure system
allows moisture transfer, the stability of the product should be determined under
conditions of high humidity at the recommended temperature (see 3.7 below).
Loss of moisture by transpiration can be important for some products, such as
intravenous infusions in plastic packs and waterbased creams in PVC tubes. The
extent of loss can be assessed by accurate weighing of marked individual packs over
time. If severe it may also be apparent as an increase in drug concentration in the
product.
Where a sponsor asserts that his container/closure system is moisture-impermeable,

evidence to this effect can be provided by, for example, the technique described in
the USPXXIII pages. 1575-1576 entitled Containers-Permeation.
2.2.7.
The possibility of leaching of substances from containers into the product should be
considered for:
- injectables and ophthalmics supplied in non-glass containers or with
plastic or with plastic or rubber stoppers,
- plastic components of metered dose aerosols, and
- any other product where this could occur and may be a hazard.
2.2.8 In-use stability data should be generated where relevant, for example:
-
where the product must be reconstituted or diluted prior to use,

where the product is claimed to be stable when mixed with other
products,
products which may be labile once the container is opened.
The stability of the in-use form of the product should be established for the period of
time and under the conditions for which storage is recommended.
Published papers may be submitted as evidence of in-use stability provided (1) they
can be shown to be relevant to the formulation proposed for registration, and (2) they
include sufficient detail to allow independent evaluation.
Where it is claimed (on the label or in product information) that the product may be
diluted with a range of solutions, the most common example being parenteral drugs
diluted in large volume intravenous infusions. Stability data should establish
compatibility with each recommended diluent at the extremes of the recommended
dilution ratios for the permitted duration of storage.
Tests on reconstituted and/or diluted solutions should normally include pH,
clarity/particulate matter, assay and, if assay sensitivity allows, degradation products.
Note however that, regardless of chemical stability, the product information for
reconstitutable and dilutable injectables should normally include the direction. To
reduce
microbiological
hazard
use
as
soon
as
practicable
after
reconstitution/preparation. If storage is necessary, hold at 2-8C for not more than 24
hours, or words to that effect. If there are valid reasons why the reconstituted and/or
diluted solution may be kept for longer periods then data should be generated to
establish the effectiveness of the preservative for the duration of the recommended
storage period.
2.2.9 Where a precipitate may form during normal storage, for example in an intravenous
injection where the drug may precipitate because of borderline solubility, directions
for redissolution must be included in product information and should be supported by
appropriate stability data.
2.2.10 Studies of container/closure interaction with the product should be considered where
this is a risk, for example injectable liquids should be stored both upright and inverted
to determine whether contact with the closure affects stability.
3. Appropriate Tests
3.1 General
3.1.1
Where test methods are identical to those in the routine quality control specifications,
this should be explicitly stated and not left to the evaluator to assume.
Alternative test methods maybe used in stability studies, but they should be fully
described and validated. Dissolution procedures other than those in finished product
specifications are discouraged.
3.1.2
If changes are made to the assay or other test method during a stability study, it may
be difficult to compare results before and after the change. On the other hand, if the
change is being made because of a deficiency in the first method, it may be
warranted. In such a case, data should be generated comparing the two methods in
terms of accuracy, precision, specificity and other relevant characteristics. Both
procedures should be conducted at several stations to find how the results compare.
Change to dissolution test methodology during stability studies are discouraged.
3.2 Assay. Details should be provided of all analytical methods used in the stability studies
together with validation data including:
- accuracy and precision in the range of the concentrations to be
measured
- shape of the calibration curve over the same range (linearity is preferred)
specificity, i.e. freedom from interference by degradation products, other
likely impurities and excipients.
It is not sufficient to determine that the drug content remains within the limits of the
specifications; the study design and assay parameters should be such as to allow any trend
over time to be observed.
As well as assay of drug, it may be necessary to assay other components, e.g. antimicrobial
preservatives. In multidose parenterals, and in some cases the content of antioxidant.
It should be noted that loss of drug may be due to factors other than degradation, such as
absorption on to or absorption into the container wall, volatilization, etc.
3.3 Degradation products. Determination of trends in formation of major degradation products
provides, in conjunction with the assay for content of drug substance, a better basis for
assigning a shelf life to a product that assay results for the drug substance alone. Therefore,
as far as possible, degradation products should be quantified or, if this is not possible,
semiquantified.
Results for content of degradation products should be provided even if the assay method is
specific for the drug. Where results are below the limit of detection of the test method, these
should be expressed as -below x%, where x% is the detection limit of the test(s) used.
Results should be given for total and all individual impurities detected, even where the identify
of the impurity is unknown. Where the identity of the impurity is unknown, results may have to
be semiquantitative.
Chromatographic techniques are preferred for the separation and detection of degradation
products, but validated alternatives methods of quantification may be acceptable. The
chromatographic system employed should be capable of separating and detecting
compounds which are likely to be present as impurities or which may arise via established
degradation pathways. It may be necessary to provide data from two or more systems to
confirm the adequacy of resolution.
Information should be provided on the means by which the methods used in the stability study
for estimating degradation products were selected.
Degradation products, present at 0.55 of the active content or greater should normally be
identified.
3.4 Physical properties. In addition to assay for content of active ingredients and degradation
products, it is also necessary to monitor the physical properties of the product during storage.
The physical tests will vary with the formation in question but important attributes of various
dosage forms may include the following:
3.4.1
3.4.2
Tablets and capsules. Dissolution rate profiles or disintegration if dissolution is not

relevant, appearance, odour, hardness, friability, moisture content, brittleness (hard
gelatin capsules).
Liquid formulations and injections. Appearance, colour, odour, pH, clarity
(solutions) and freedom from visible particulate contamination, size range of
particulate contamination large volume parenterals),
particle size distribution
3.4.3
3.4.4
3.4.5
3.4.6
3.4.7
(suspensions), micelle size distribution (micellar solutions), resuspendibility

(suspensions), viscosity, moisture content (powders for reconstitution), phase
separation (emulsions).
Ointments and creams. Appearance, odour, viscosity, softening range, loss of
water, physical and chemical homogeneity, particle size distribution, particle
formation, pH.
Freeze-dried material. (including materials for reconstitution). Appearance of both
freeze-dried and reconstituted material, pH, water content, rate of solution.
Aerosols. Leak tests, particulate contamination, valve function and appearance,
weight loss. Metered dose aerosols, and some pump actuated aerosols, will also
require measurements of drug mass aerodynamic particle size distribution on aging.
Suppositories and pessaries. Appearance, softening temperature (moulded
products), dissolution rate (compressed products).
Transdermal patches. Appearance, in vitro release rate.
3.5 Preservative efficacy. Because chemical assays do not necessarily indicate antimicrobial
efficacy, if a product is required to contain an antimicrobial preservative, for example eye
drops or multidose injections, it will usually be necessary to conduct a microbial challenge test
at the end of the shelf life in addition to chemical assay of the preservative during the study.
3.6 Dissolution rate. The behavior of dissolution rate over time should be examined for all solid
oral dosage forms and other compressed products (suppositories, implants, etc.) even where
the drug is water soluble. Dissolution data should normally be generated on at least six
individual units at each test station (e.g. 1 month, 3 months, 6 months etc) and should be
reported as both individual and mean data. Test conditions should normally be those used in
routine quality control or, if dissolution is not a part of routine quality control, any reasonable,
validated method.
It may be necessary to generate dissolution profiles (percent of nominal content dissolved at
a number of time points at appropriate intervals to almost complete dissolution) for certain
products, for example:
-
modified release products.

certain immediate release products, for example carbamazepine tablets
where it has been shown that tablets which release the drug rapidly lead
to a higher incidence of adverse effects,
in cases where there are doubts as to the validity of the dissolution test
method,
in cases where single point data suggest there any be a problem with the
dissolution rate of the product, especially with aging.
3.7 High Humidity Studies. The use of plastic containers for the packaging of pharmaceuticals
raises questions concerning the stability of the contents when stored under conditions of high
humidity. High relative humidity can affect chemical stability (for example some antibiotics are
readily hydrolysed) and physical stability (for example, altered dissolution rate).
Date should be generated to establish the effect of high humidity on solid dosage forms
packaged in containers which are likely to be permeable to moisture. This includes containers
made from polyvinyl chloride or low density polyethylene but does not include those made
from glass or high density polyethylene. If a sponsor believes that high humidity data are not
needed for a product which is packed in a plastic material, this view should be supported by,
for example, information on the composition, thickness, density and/or moisture
transmissibility of the packaging materials.
Temperature and relative humidity data available from the Bureau of Meteorology have
established that a number of centres in Philippines experience a combination of high humidity
and high temperature during the summer months.
Satisfactory stability results when the product is stored at 25C and 80% RH or 30C and 75%
RH for 3 months are normally sufficient to establish the adequacy of the packaging to protect
the product from moisture for a period of up to 2 years. Data which show stability for a period
of 6 months are normally sufficient to support shelf lives in excess of 2 years.
These short term high humidity data provide support for stability data accumulated at the
maximum recommended storage temperature at lower relative humidity, but do not obviate
the need for studies for the duration of the shelf life.
4. Presentation of Results
4.1 Results obtained at the commencement and at nominated time intervals throughout the trial
(for example 0, 3, 6, 9, 12, 18, 24 months, or 0, 1, 2 and 3 months for high humidity studies)
should be provided. This will allow any trends to be detected and will enhance the predictive
value of the trial.
Data which do not include initial results (that is at the start of the trial) are of limited value.
4.2 If more than one assay result is available for any particular time interval, all results should be
quoted rather than, or in addition to, an average figure. Where bioassays are employed to
study antibiotics, the accompanying fiducial limits of error (p=0.95) of each assay should be
provided.
4.3 Assay results obtained during the study should be recorded either as absolute values (such
as number of mg of drug per capsule) or as a percentage of the nominal (labeled) content.
4.4 Care should be taken that individual dose unit variations, such as between individual tablets
or between individual vials of freeze-dried powder, are allowed for in stability studies. For
freeze-dried vials, this may be achieved by assaying the content of active per unit weight of
powder. For tablets and capsules, an average content may be obtained by conducting the
assay on pooled samples (normally 20 tablets or capsules), or by averaging individual dose
unit results.
4.5 Wherever possible, quantitative results should be quoted rather than a statement that the
product complies with a particular specification.
4.6 All results obtained should be discussed and explanation given where necessary, for example
anomalous or unusual results, change in assay method, change in appearance.
4.7 A brief outline of the sampling procedure followed in the stability trial should be provided.
5. Prediction of Shelf-Life from Stability Data

One of the more difficult steps in a stability trial is to assign appropriate storage conditions and a
shelf life from the accumulated data. The difficulty is reduced and the reliability of extrapolation
enhanced if the data include frequent intermediate stations, are derived from several batches,
consider a range of conditions, are high precision, include analysis for breakdown products and
consider the physical properties of the formulation.
The accumulation of stability data is a lengthy procedure and it is sometimes necessary to predict
a probably shelf life for a product stored at a defined temperature from stability data obtained at
an elevated temperature. This accelerated stability testing is useful in providing information from
which to assess the probable stability of a new product but it should be conducted in conjunction
with long term stability studies at the maximum recommended storage temperature for the
duration of the nominated shelf life.
In theory, the stability of the drug substance is directly related to the kinetics of the various
degradation reactions. However the relevant physicochemical equations are strictly applicable
only when a single reaction occurs be a single mechanism. Because pharmaceutical products are
usually mixtures of substances and may be in the solid state (for example, powders and tablets),
these theoretical models do not necessarily hold and cannot be relied upon as predictive tools.
The issue of physical stability (for example dissolution rate and particle formation) adds a further
complication. There is therefore no substitute for the shelf life being determined empirically
ultimately over the full shelf life.
The following general rule-of-thumb is used by the evaluators when assessing data from elevated
temperature studies:
If no trends are noted after storage for a period of (x) months at an elevated temperature (at least
10C above the maximum storage temperature proposed for the product) then an interim shelf life
of a maximum of 2(x) months may be permitted, where 2(x) does not exceed 3 years.
Shelf lives of longer than 3 years should be supported by data on production batches stored at
the maximum recommended temperature for the duration of the proposed shelf life.
Stability trials involving at least three production batches stored at the maximum recommended
temperature should in any case be continued for the full period to validate the predicted shelf life.
Interim shelf lives may be extended through submission of additional data accumulated in the
later stages of the trial. Manufacturers should not however that the shelf life may not be extended
until the data have been evaluated be BFAD and a new shelf life agreed.
6. Product Modifications
Manufacturers may not implement changes to pharmaceutical data without prior approval by
BFAD. Applications to make changes should provide details of the proposed change and relevant
pharmaceutical data to the PSD. Whether or not stability data are required will be a matter of
judgment in each case.
These are examples of changes which would normally require supporting stability data:
-
a change to the pH specifications of a liquid product.

change of tablet container from a glass bottle to a PVC blister.
a change in the synthetic route for the active raw material together with changes in impurity
levels.
an increase in the radioactive concentration at which a radiopharmaceutical is provided.
The following are examples of changes which would not normally require justification in terms of
additional stability data provided that adequate stability data are available for the existing product
(note however that data other than stability data may be required):
- tightening of existing specifications for the drug product consistent with existing stability data,
for example narrowing of assay limits for a drug,
- change of site of manufacture of the active raw material or finished products with no other
change to pharmaceutical data,
- an additional pack size for tablets stored in a blister pack with no change of packaging
materials.
The following general comments may assist sponsors in the accumulation of stability data in
particular circumstances.
6.1 Change in Formulation. A proposed to change to a completely new formulation would be
regarded as an application to register a new product and would require
6.2 Change in Packaging. The major consideration in evaluating a proposal for a change in
packaging is the relative protection afforded the product by the new and old packs. If the new
pack is shown to be more protective, e.g. an amber screw-capped glass bottled compared
with a clear PVC bottle, it is likely that no data would be required. Where the pack is less
protective or where some interaction with the container is possible, additional stability data will
be required.
For parenteral or opththalmic solutions in new plastic packs, information on leaching is
important. Appendix XIX of the BP 1993 and <661) of the USP XXIII (1995) provide an outline
of some of the factors to be considered and test methods. Where the new pack has a greater
permeability to moisture, the effects of high humidity on solid dosage forms or the extent of
possible fluid loss from liquid preparations should be considered.
7. Prospective Extensions of Shelf-Life for Individual Batches
Under certain circumstances BFAD may approve a limited extension of shelf life for individual
batches approaching there expiry date in the absence of the stability data that may normally
be necessary. The prerequisites are as follows:
7.1 the existing shelf life should be at least 2 years
7.2 stability data should be available to BFAD which validate the existing shelf life and show
no deterioration of the product during this product
7.3 a recent (less than 2 months old) dated certificate of analysis should be supplied for the
batch showing compliance with specifications, together with the results obtained at batch
release
7.4 the company should provide an assurance that it has commenced or intends to
commence a stability study to validate a permanent extension of the shelf life
8. Shelf-life Extensions According to an Approved Protocol
Shelf lives may be extended in accordance with a stability test protocol which was approved
explicitly for this purpose. Such protocols may be submitted with the application for registration or
subsequent to registration. All of the following conditions apply:
8.1 BFAD must have explicitly approved the protocol for the purpose of self-assessable shelf life
extensions.
8.2 All pharmaceutical aspects of the product, including its immediate container and closure and
labeled storage conditions, are identical to those approved at the time a stability test protocol
was approved, except for changed made in accordance with other parts of this document.
8.3 At least two production batches of the product have been tested in accordance with the
approved stability test protocol.
8.4 The total shelf life is not longer than the time for which stability data meeting the approved
protocol are available on two production batches, and in any case is not longer than 5 years.
8.5 If BFAD requests copies of the additional stability data, these will be supplied within one
month of the request.
8.6 Any stability test protocol proposed for this purpose should include:
8.6.1 A statement of the proposed tests and test methods.
8.6.2 A matrix indicating the time stations at which each of the tests will be conducted.
8.6.3 Acceptable limits for results for each test
Note that:
-
BFAD may impose conditions on the implementation of an approved test protocol, such
as a maximum total shelf life of less than 5 years and
To provide a suitable safety margin, the acceptable limits for results should be somewhat
tighter than expiry specifications. If results are outside these tighter limits but within expiry
specifications, the sponsor has the option of submitting the data for evaluation with an
argument as to why the shelf life should be extended.
Stability Guidelines Appendix I

Acceptable Temperature Storage Conditions Which may Appear on Labels
1.
2.
3.
4.
5.
6.
Store below - 18 C (Deep freeze)

Store below - 5oC (Freeze)
o
Store below - 8 C (Refrigerate)
o
Store below - 8 C (Deep freeze)
o
Store at 2 to 8 C (Refrigerate. Do not freeze)
o
Store below - 25 C
Stability Guidelines Appendix 2
Common Deficiencies in Stability Data and Trial Design

To assist sponsors in the design and reporting of stability studies, a list of deficiencies which are
commonly encountered and which lead to question and delays in approval of a shelf life are given
below.
1. Failure to specify the formulations used in the trial, and to state which batches are identical to the
formulation that will be registered in the Philippines.
2. Failure to state whether the batches used in the trial were the pilot or production batches.
3. Failure to describe clearly the packaging used in the trial and to confirm whether it is identical to
the pack which will be used in the Philippines.
4. Failure to accumulate stability data or more than one batch of the product.
5. Failure to define accurately the temperature, lighting and humidity conditions applied during the
trial.
6. Failure to fully describe test methods and samples sizes.
7. Failure to provide validation of analytical methods
8. Expression of results as passes test or similar when a quantitative figure would be available.
9. Failure to include quantitative or semiquantitative determinations of the content of degradation
products, or to provide only total content rather than values for individual impurities.
10. Use of an HPLC assay procedure to detect impurities without validation for the purpose. HPLC
assay procedures as used for determination of the active ingredient are often unsuitable for
separation and detection of Impurities as they use too short a run time. Such a procedure would
be acceptable if validated for impurity detection. (Note, however, that long run times do not in
themselves ensure good separation.)
11. Failure to comment or conduct additional tests when there is a lack of mass balance between the
formation of degradation products and the loss of the active substance. For example, are the
assay procedures sufficiently specific? Is the drug volatile? Is it adsorbed on to the container
wall?
12. Failure to conduct additional tests to investigate the significance of obvious alterations in the
characteristics of the product. For example a distinct change in the colour of the product may
necessitate additional investigation for degradation products.
13. Failure to include information on the physical characteristics of the product during storage, such
as dissolution characteristics, homogeneity, particle size etc.
14. Failure to reconstitute radiopharmaceuticals at the activities and radioactive concentrations that
would be used in a clinical situation.
15. Failure to include stability studies under conditions of high humidity for products which are to be
registered in moisture permeable containers, and especially for those which are potentially labile
to moisture such as antibiotics.
16. Failure to provide results from intermediate time stations to facilitate assessments of any trends in
the parameters measured.
17. Failure to provide results for individual dosage units where these are available, for example
dissolution profiles.
18. Attempting to extrapolate data obtained in the trial beyond reasonable limits.
Stability Guidelines Appendix 3

Glossary of Terms
Active Raw Material: The unformulated active chemical substance, usually a powder or a liquid, in
the form in which it is used to manufacture the dosage form, usually in combination with excipients.
Direct Scales: Products are said to be direct scales if the same granulated or mixture of powders is
used to manufacture the various strengths, but the products are compressed or filled at varying
weights corresponding to the various strengths.
Dosage Form: The pharmaceutical form in which a product is presented for pharmaceutical
administration, for example, tablet, injection, cream, suppository, etc. Note that modified release
formulations are not the same dosage form as their conventional counterparts, for example, a
sustained release tablet and a conventional tablet: a depot injection and an aqueous solution for
intramuscular injection.
Finished Product: For the purposes of this document, the finished dosage form when all stages of
manufacture have been completed to the stage of packaging in the immediate container (e.g.
ampoule, tube, sachet, blister etc.)
Labels: The labels on the container (e.g. ampoule, tube, sachet, blister etc) and on any carton or
other overwrap which is part of the primary pack.
Impurity: An unintended component of a substance or product. Impurities include degradation
products, by-products of chemical synthesis and contamination from any other source. A degradation
product may be an isomer, for example, following racemisation.
Pharmaceutical Data includes:
-
the method of synthesis or biosynthesis, proof of structure and purification of the active raw
material
the formulation, method of manufacture and stability of the finished product
specifications (including test methods) of the active raw material, excipients and finished
product
labelling, including shelf life, storage conditions and recommendation for processing prior to
use (e.g. reconstitution of a powder for injection)
bioavailability as applicable
Pilot Production Batch: A quantity of product which is identical in formulation and equivalent in
terms of manufacturing equipment and manufacturing method to a production batch, except for scale.
Semiquantitation: ballpark assays and therefore less desirable than true quantitation. Two
techniques are common:
1. for unknown impurities, a result is assigned on the basis of comparison with known
concentrations of the drug substance, e.g. by colour depth on a TLC plate. This technique is not
preferred as (1) the assumption of similar physicochemical properties for the degradation product
and the drug substance may be incorrect, and (2) even if the assumption is correct, the technique
is only approximate. It is generally used only in cases where the degradation product has not
been identified and is present in only trace amounts.
2. where the degradation product has been identified but is present in very small quantities, a result
is assigned on the basis of comparison with known concentrations of the authentic degradation
product.
In both cases, results are expressed as, for example, less than 0.055 or between 0.01 and
0.055. Expression of results as trace amounts is discouraged as there should normally be some
estimate of the limit of detection.
Stability Guidelines References
1. British Pharmacopoeia 1993 Department of Health and Social Security, UK (1993)

2. United States Pharmacopoeia XXIII United State Pharmacopeial Convention (1995)

Bureau Circular 5 S 1997

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Republic of the Philippines

March 19, 1997

: ALL DRUG ESTABLISHMENTS AND PARTIES CONCERNED

: REVISED CHECKLIST OF REQUIREMENTS AND THE 1997

(Sgd) QUINTIN L. KINTANAR, M.D., Ph.D.

FILING OF APPLICATION FOR REGISTRATION

A pre-assessment of the application shall be conducted by a PSD evaluator at the PAICS

REQUIREMENTS FOR INITIAL REGISTRATION

Certificate of Brand Name Clearance

the specific activity(ies) that each shall undertake relating to the

Unit dose and batch formulation

Technical/Quality Specification of all Raw Material(s)

The current edition of the United States Pharmacopoeia/National

The technical/quality specifications of ingredients not described in

adversely affect the stability of the medicinal product or distort

Certificate of Analysis of Active Ingredient(s)

Technical/Quality Specifications of Finished Product

Certificate of Analysis of the Finished Product

In case of continuous manufacture, full details concerning precautions taken

3.1.12 Detailed report of stability studies to justify claimed shelf-life

4. The drug product applied for requires special handling.

3.1.17 Bioavailability/Bioequivalence Studies for products under List B (As

NEWLY INTRODUCED DRUG

Application for Initial Registration shall comply

Certificate of the Medical Director registered with BFAD

Reference Standard and its corresponding Certificate of Analysis

Acute toxicity data should be able to:

define the intrinsic toxicity of the drug

Lethal dose 50 (LD50)

2. Evaluate the effects of the drug on reproduction when given

(c) Litter as to number of pups (litter size), weight of pups,

2. Clinical Investigation Data

scientific training and

d. The investigators must observe the regulations regarding

Application for Initial Registration shall comply with the following

Local Clinical Trial (optional)

Application for Initial Registration shall comply with the following

Phase III Clinical Drug Trial (optional)

Local Clinical Trial (optional)

3.5 PRODUCTS WITH NEW DOSAGE FORM

Application for Initial Registration shall comply with the following

10. Sufficient samples in market or commercial presentation for

Bioavailability or Bioequivalence Data, as needed

3.6 PRODUCTS WITH CHANGE IN:

3.8 PHASE IV CLINICAL TRIAL FOR PRODUCTS UNDER THE FOLLOWING

4.2 Application for renewal registration of drug or pharmaceutical specialty shall be

A surcharge of 50% or renewal registration fees shall be imposed

The active and inactive ingredients should be pharmaceutically (i.e. chemically,

(Sgd) QUINTIN L. KINTANAR, M.D., Ph. D., CESO l

GUIDELINES ON THE STABILITY TESTING OF PHARMACEUTICALS

products containing drugs which are prepared by chemical synthesis

The product should be tested in the container/closure system in which it will be

Stability information should be generated on a minimum of three batches. Where this

Conditions of storage likely to be encountered in the Philippines should be considered

Where the product is to be registered in a moisture permeable material such as

Where a sponsor asserts that his container/closure system is moisture-impermeable,

where the product must be reconstituted or diluted prior to use,

Tablets and capsules. Dissolution rate profiles or disintegration if dissolution is not