Organising a Regulatory Workshop for Medical Devices and IVDs

16658

Event Info:

12th Apr 2024

10:00 am - 03:00 pm

Venue:

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Contact:

info@ikp.com

Slots Available:

35 slots available out of 40

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On 21st July, the IKP Global Regulatory Forum (IGRF) organised a regulatory workshop for medical device start-ups at T-Hub in Hyderabad in collaboration with Research and Innovation Circle of Hyderabad (RICH).

Dr. A. Ramkishan, Deputy Drugs Controller (India), Central Drugs Standard Control Organisation (CDSCO) Hyderabad; Ms. Sarala Devi, Assistant Drugs Controller (India), CDSCO Hyderabad; and Dr. P.V. Appaji, Emeritus Director General, Pharmaceuticals Export Promotion Council of India (Pharmexcil) provided insights to start-ups on the support available for them in this sector, and talked about the MDR 2017 requirements for medical devices and IVDs.

Mr. Kamal Prasad, Founder and Director of PathnSitu Biotechnologies, put forth the specific queries of start-ups attending the workshop and explained the details of the Device Master File (DMF) alongside IKP’s Dr. Priyankana Mukherjee.