Regulatory Information Facilitation Center is happy to announce R-Clinic for Medical Device Startups, a unique opportunity to gain personalized regulatory insights and accelerate your path to market!
Details -
- Date: 18th February 2025
- Time: 2:30 PM - 4:30 PM
- Mentoring session: 30 mins per startup Limited Seats
- Mode: Online
About the mentors:
- Chetna Dabi: Chetna works for the Regulatory Information and Facilitation Center (RIFC) at Venture Center and assists various medical device startups in planning regulatory pathways, interpreting standards, and establishing and implementing a quality management system for medical devices. She is a certified lead auditor for ISO 9001 and ISO 13485 QMS.
- Akash Dhade: Akash works for the Regulatory Information and Facilitation Center (RIFC) at Venture Center and assists multiple organizations in choosing regulatory pathways, creating technical documentation, and submitting the documentation to the notified bodies for the European market. He has experience drafting over 20 technical documentation for different types of medical devices and also has the lead auditor certification for ISO 13485 QMS by BSI Academy.
For more information, contact us at aishwarya.varpe@
