##  [Indian Medical Device Regulatory Landscape - A Deep Dive](/webinars/indian-medical-device-regulatory-landscape-a-deep-dive) 

<a>Medical Devices</a>



<a>Past Webinar</a>



## **Indian Medical Device Regulatory Landscape - A Deep Dive**

**The webinar was successfully concluded on**

  **September 22, 2021.**

[Download Webinar](javascript:void(0))





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 Here is an archived version of the session for your perusal.

#### What Was It All About?

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.