Indian Medical Device Regulatory Landscape - A Deep Dive
We are delighted to see your interest in Freyr’s Webinar Series (FWS). The webinar on “Indian Medical Device Regulatory Landscape- A Deep Dive” was successfully concluded on September 22, 2021. Here is an archived version of the session for your perusal.
In the session, our in-house Regulatory expert, Sushma Yedunuri, Head - Indian medical device projects, elaborated on:
Indian Medical Device Industry- Background
Indian Medical Device Regulatory Landscape - Current Scenario, Timeline, the CDSCO Initiatives
Terms - Notified and Non-notified Devices and List of Notified Devices
Different Registration Pathways for Medical Devices- Listing, Import, Manufacturing License
Registration Listing of Non-notified Medical Device
As a continuous practice, Freyr is destined to organize more webinar sessions related to Regulatory aspects of Life Sciences. We presume that you would like to be a part of all the upcoming sessions. If yes, let us have an opportunity to inform you about our next session.