Tentative Annual Schedule of the Clinical Studies Committee (CSC) Meetings for the year 2026

The Clinical Studies Committee (CSC) of the Drug Regulatory Authority of Pakistan (DRAP) is constituted under the Bio-Study Rules, 2017 to provide regulatory oversight of clinical trials and other clinical studies relating to therapeutic goods in Pakistan. The Committee reviews and approves clinical study protocols to ensure compliance with applicable ethical, scientific, and regulatory requirements. It also oversees the conduct of approved clinical studies, monitors participant safety and study progress, and makes informed decisions on matters pertaining to the design, conduct, and oversight of clinical research. In carrying out its mandate, the CSC collaborates with researchers, sponsors, and other stakeholders to promote high-quality clinical research while safeguarding the rights, safety, and well-being of study participants.


To enhance transparency, efficiency, and coordination in the conduct of its business, the Clinical Studies Committee has decided that its meetings shall ordinarily be convened at intervals of approximately forty-five (45) days. Accordingly, the tentative Annual Schedule of CSC Meetings for the year 2026 has been issued.


Notwithstanding the tentative annual schedule, the Chairman, CSC, may convene meetings of the Committee at any time, as deemed necessary, to address urgent or emerging regulatory matters.

S. No.CSC MeetingProposed Dates for CSC Meeting
0161st CSC Meeting2nd week of April 2026.
0262nd CSC Meeting2nd week of May 2026.
0363rd CSC Meeting3rd week of June 2026.
0464th CSC Meeting2nd week of August 2026.
0565th CSC Meeting3rd week of September 2026.
0666th CSC Meeting3rd week of October 2026.
0767th CSC Meeting3rd week of November 2026.
0868th CSC Meeting3rd week of December 2026.

FIFO lists of applications received for enlistment of Herbal, Homeo ,  Neutraceutical  products (Year 2024)

DISCLAIMER
“The FIFO list for year 2024 of alternative medicines and health products is prepared with due diligence for transparency of process and visibility of the stakeholders. However, errors and omissions may be accepted subject to valid evidence.”

Herbal

Homeo

Neutra

DRAP Newsletter: Volume 03-Issue -II, November, 2024

The Drug Regulatory Authority of Pakistan (DRAP) has released a new issue of its quarterly newsletter, featuring several key updates and initiatives. DRAP has extended the scope of its Industry E-Reporting System for Adverse Drug Reactions to all registration holders, following a successful pilot project. The newsletter details recent actions on the promotion of clinical trials regulatory oversight, the stakeholder queries management system, and interprovincial coordination for the implementation of the Institutional Development Plan as per WHO recommendations. Additionally, the newsletter covers ongoing efforts to enhance public health and safety, including increased surveillance and regulatory actions to ensure the quality and safety of therapeutic goods.