We appreciate your interest in Freyr’s Webinar Series (FWS). The webinar on “Indian Medical Device Regulatory Landscape – Current Dynamics” will be held on February 22, 2023, for AMR, EUA & ROW regions.

What Is It All About?

The medical device industry is considered one of India's fastest-growing markets. The Indian Regulatory authority CDSCO makes an assiduous effort to enhance its Regulatory framework to introduce effective and safe medical devices to the market.

Do you comprehend India's current Regulatory dynamics, relevant regulations, and various device registration procedures as a device manufacturer? To assist you in better understanding the wide Regulatory landscape of the Indian medical device industry, we are presenting you with an exclusive webinar:

Indian Medical Device Regulatory Landscape - Current Dynamics

February 22, 2023

Duration – 45 Minutes

Join the Webinar at your Convenient Time

For AMR & EUA Regions

10:00 AM EST | 04:00 PM CET

For RoW Region

11:30 AM IST


Kristen Laudicina​

Vice President of Strategic account, Medical Devices​

Kristen Laudicina is the Vice President of Strategic Account for Freyr’s Medical Devices Center of Excellence (CoE). She oversees the North and South American Regions and supports Freyr’s Medical Device CoE team. Kristen has 12+ years of experience within Life Sciences, from Preclinical through Commercial Manufacturing, and understands the client’s needs from both a Sponsor and Service Provider perspective.​


Sravanthi Mingi​

Senior Manager, Indian Medical Device Regulatory Affairs

Sravanthi Mingi has over 10+ years of experience in the field of Regulatory Affairs with rich expertise in diversified medical device categories. She has worked with organizations ranging from small start-ups to multinational corporations. She is one of the experts on Indian medical device regulations and has assisted many device manufacturers in registering their devices with CDSCO and other multiple Health Authorities. Her core area of expertise involves developing Regulatory strategies during the development of devices, submission strategies and overseeing Regulatory submissions throughout device approval. Sravanthi graduated from Orebro university with a master's in Biomedicine.​

In this webinar, our in-house Regulatory expert - Sravanthi Mingi – Senior Manager, Indian Medical Device Regulatory Affairs, will elaborate on the following:

  • History and overview of the Indian medical device industry
  • Indian medical device Regulatory dynamics
  • Registration of medical devices and IVDs with CDSCO
  • New regulations and amendments to the Medical Device Rules, 2017
  • Case studies
  • FAQs

Given the keynotes and with due consideration for your hectic schedule, we anticipate seeing you at the webinar. Register now! Stay informed. Stay compliant.

For AMR & EUA Regions

10:00 AM EST | 04:00 PM CET

For RoW Region

11:30 AM IST

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