Regulatory Information and Facilitation is happy to announce an Awareness Talk on the FDA’s Quality Management System Regulation (QMSR) Final Rule for medical device manufacturers.
What to expect:
- Introduction to QMSR and its purpose
- Differences between 21 CFR Part 820 and ISO 13485
- Compliance timeline and transition strategy
- Impact on medical device manufacturers
- Best practices for QMS alignment
- Live Q&A with the expert
Date: 22 April 2025
Time: 11:00 AM – 12:00 PM IST
Mode: Zoom (Online)
Speaker: Akash Dhade (Associate Manager – Regulatory Services)
Register Now
(Email invites along with a session joining link will be sent one day before the event.)
For more information contact: Aishwarya Varpe | aishwarya.varpe@venturecenter.co.in | 9156465137
