DRAP
The new article describes in detail the key responsibilities of the parties involved in clinical research.
DRAP
The article provides a general overview of Pakistan’s regulatory requirements for clinical research.
Asia
The article provides a brief overview of Pakistan’s regulatory requirements in the sphere of importation and exportation of medical devices and highlights the key points to be considered by medical device manufacturers and other parties involved in placing medical...
Asia
For the last 70 years, only a handful of medical devices have been regulated in Pakistan under its Drug Act of 1976. In an attempt to control the quality of the devices being sold and used in the country, the Drug Regulatory Authority passed the Medical Device Rules...
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