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