What is ISO 13485:2016? How is it related to 5th schedule of Indian Medical Device Rules 2017? How willl a certification ease your road to commercialing your med device?
Medtech developers, don't miss this second webinar in the Med Device management series by CCAMP and BIRAC-DBT National Biopharma Mission supported Medtech Rapid Prototyping Facility uFab.
A webinar on ISO 13485:2016: An Overview with Siddharth Jain, CEO & Chief Medical Device Regulatory Affair Advisor, Symbiorph Clinical Trialogy
Date & Time: April 12, 2-4pm
Register: https://docs.google.com/forms/d/e/1FAIpQLSfoKmo2NTh1J-0lIXGBoEfUSgg1XndLXEUWmywnqeqDUMFpdw/viewform by April 5th, 2021
Monday, April 12, 2021