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.
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:
February 22, 2023
Duration – 45 Minutes
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.
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:
Given the keynotes and with due consideration for your hectic schedule, we anticipate seeing you at the webinar. Register now! Stay informed. Stay compliant.