Module 11 UHC 2024
Module 11 UHC 2024
Module 11 UHC 2024
The independent technical body duly authorized and delegated by the Secretary of Health to provide technical advice and
guidance to the DOH in implementing appropriate measures that promote and ensure access to affordable quality drugs and
medicines for all consumers in the Philippines:
A re-negotiation may be conducted as deemed appropriate by the end-user before the expiration of the Memorandum of
Agreement based on a set of criteria that includes the following:
The DOH office responsible for the review of the medicines to be included in the Primary Care Formulary:
The following is responsible to synthesize the data submitted by the end-user and Health Technology Assessment Council:
The following statements are correct for successful outcomes of price negotiation, EXCEPT:
a. Companies are given fifteen (15) working days upon receipt of the decision of the Board to submit an appeal.
Ongoing expense of operating a business that cannot be conveniently traced to any particular cost unit:
a. Overhead cost
The following are true in the imposition of maximum retail price (MRP) on drugs and medicines:
The following statements are correct regarding the computation of retail prices for highly specialized drugs:
Drug or medical device that has been granted intellectual property rights, which provides a legal right to exclude others from
making, using, selling, and importing for a limited period of years:
The following are the objectives of the Administrative Order 2020-0043 (Guidelines on Ensuring the Affordability of Essential
Medicines in DOH Facilities Through the Regulation of Price Mark-ups):
The following are true regarding generic alternatives of drugs and medicines:
The following are the benefits of centralized price negotiation thru the Price Negotiation Board:
The following strategies are aimed to make price information of all health goods and services available and accessible, EXCEPT:
The following are the criteria being used by the Drug Price Advisory Board for selecting drugs and medicines for consideration
under maximum retail pricing, EXCEPT:
Unit cost reflected in the Purchase Order which is the basis in the computation of price mark-ups:
a. Acquisition cost
As provided in the UHC Act, drugs and medicines listed in the Primary Care Formulary (PCF) shall have fairly priced generic
equivalents. The formulation of the PCF shall be based on:
The following agencies must have representatives as members of the Price Negotiation Board, EXCEPT:
a. FDA
Drug or medical device that is used, produced, or marketed under exclusive legal right and protected by patent:
The following prerequisites and preparation apply for health commodities that are already listed in the Philippine National
Formulary:
The prices of the following shall be included in the list of price information in all DOH-owned health facilities:
The following statements are true regarding the guidelines on public access to price information of all health goods and services
in DOH-owned health facilities:
In the implementation of price mark-ups in DOH-owned health facilities, the following is responsible to endorse to the
Commission on Audit any report of non-compliance observed by the Internal Audit Service:
The following statements are correct regarding price mark-ups of drugs and medicines in DOH-owned health facilities, EXCEPT:
a. Random monitoring of medicines prices shall be done regularly at DOH-owned facilities by the FDA.
Consumer’s guide that provides information on where to get the cheapest medicines within their area:
The following statements are true regarding the appeal of any health facility whose license or accreditation is revoked or
suspended due to noncompliance to the provisions of Administrative Order 2021-008 on public access to price information of all
health goods and services, EXCEPT:
a. The decision of the Head of DOH HRT shall be final and executory.
Drug or medicine with an active pharmaceutical ingredient or molecule that was first originally marketed globally:
a. Comparator drug
The following statements are true regarding the composition of the Drug Price Advisory Board, EXCEPT:
The countries used as the basis for external reference pricing in determining the maximum retail price of drugs and medicines:
The agency responsible to investigate alleged violations of Maximum Retail/Wholesale Price of drugs and medicines in
accordance with relevant laws:
In the implementation of Maximum Retail Price (MRP), the Department of Trade and Industry is responsible for: