Indian Pharmaceutical and Medical Device Regulation 101

Episode Introduction: In this podcast, Darren Punnen, senior member of the pharmaceutical and lifesciences practice at NDA, provides an overview of how every aspect of the pharmaceutical and medical device industry is regulated. This includes the clinical trial, manufacture, import, packaging and sale of medical devices. He also covers ancillary drug regulation such as the drug price control legislation, the drug advertisement legislation and the regulations applicable to healthcare practitioner in so far as they impact pharmaceutical and medical device companies. Some of the legislations covered include.

CONTINUE READING ON www.natlawreview.com