Good Pharmaceutical Practices On
Good Pharmaceutical Practices On
Good Pharmaceutical Practices On
ASSINGMENT ON
Good Pharmaceutical Practices On Compounding And Dispensing
Submitted To Submitted By
Rabeya Jafrin Mou Tabassum Rajoana Tumpa
Lecturer
Department of Pharmacy ID: 201 052 032
Primeasia University
Department of Pharmacy
Primeasia University
Date of Submission:19-12-2021
Good Pharmaceutical Practices On
Compounding And Dispensing
Compounding
Drug compounding is often regarded as the process of combining, mixing, or altering
ingredients to create a medication tailored to the needs of an individual patient. Compounding
includes the combining of two or more drugs. compounding pharmacy is an important ally in
providing access to discontinued or hard to find medications.
Dispensing
Dispensing is the provision of drugs or medicines as set out properly on a lawful prescription.
The dispensing of drugs should be carried out by trained pharmacists. Dispensing is the
provision of drugs or medicines as set out properly on a lawful prescription. Dispensing is one of
the vital elements of the rational use of medicines.
Good Pharmaceutical Practice means the standards that are generally accepted by the
pharmaceutical community as constituting appropriate and adequate care. GPP is the practice
of pharmacy that responds to the needs of the people who use the pharmacists' services to
provide optimal, evidence-based care. The purpose of this standard is to provide guidelines to
pharmacists and PSP when medicines are dispensed or re-dispensed as individual unit doses for
a particular patient, to facilitate administration with the aim of improving adherence to
therapy.
Practices Compounding
Preparatory
• Judging the suitability of the prescription in terms of its safety and intended use and the dose
for the patient.
• Assembling all the necessary materials and ingredients to compound and package the
prescription.
Regulation
In contrast with the practice today, regulatory bodies exist for pharmacy practice and
compounding. One of their jobs is to produce regulation, uniform standards, and guidelines to
guarantee that only the highest quality products are prepared for the patients and to ensure
patient health and safety. Regulatory bodies are in charge of creating regulations and making
existing regulations striken so as to ensure the safety of patients.
Sign-Off
Signing and dating the prescription, affirming that all of the indicated procedures were carried
out to ensure uniformity, identity, strength, quantity, and purity.
Final Check
Checking, as indicated, the weight variation, adequacy of mixing, clarity, odor, color,
consistency, and pH.
Labelling
Labelling should be done according to state and federal regulations. labelling information
includes the:
Personalizing compounding
Compounding has further evolved into more innovative practices, such as customized dosages,
alternative drug delivery systems and production of allergen-free formulations.
Screening of Prescription
• On receiving a prescription, it should be screened and validated to ensure that it is for
the correct patient and it complies with the requirements in the Poisons Act.
supply of medicine
When dispensing the medicines, ensure the 5Rs:
Right Patient
Right Medicine
Right Dose
Right Route
Right Time
A safe, clean and organised working environment provides the basis for good dispensing
practice. The dispensing environment includes-