Our Functions

Drug Regulatory Authority of Pakistan (DRAP)
is providing following functions in particular

Regulatory functions

Drug Registration
Biological Registration
Medical Devices Registration

Guide Lines

cGMP Guidelines
Guidelines for Enlistment and Alternative Med,Pharma Units

Checklist

Checklists for Inspections of Drugs Manufacturing Premises
Inspections of Drugs

Functions For

Health Products Registration
Alternative Medicine,Drug Manufacturing Units

Imported Drugs

Storage for Imported Drugs

Biological Manufacturing

Inspections of Biologicals Manufacturing

GUIDELINES ON GOOD DISTRIBUTION PRACTICE FOR MEDICAL DEVICES (GDPMD)

Distribution is an important activity in the integrated supply-chain of medical devices. Various personnel and entities are generally responsible for the product sourcing, procurement, transportation, delivery, storage, device tracking, installation, commissioning, service and maintenance and calibration need to be appropriately managed and controlled to ensure the safety and performance of medical devices at the point of use.
The Guidelines on Good Distribution Practice for Medical Devices (GDPMD) is developed to elucidate the requirements for an appropriate management and control of these activities

GUIDELINES /STANDARD OPERATING PROCEDURE

Applications of controlled substances shall be submitted for each year by the firm/applicants by 7th January, with data consumed till 31st December of previous year
Checklist submitted with application shall be duly signed by MD / CEO / authorized senior representative and should also clearly indicate percentage of consumption (manufacturing and sale).