Behind every successful MedTech innovation is a strong regulatory foundation — this initiative offers startups practical guidance on navigating approvals, compliance, and market pathways through focused one-on-one interactions.
The Regulatory Information and Facilitation Center (RIFC) at Venture Center is happy to announce R-Clinic for Startups developing Medical Devices, SaMD, or IVDs, a unique opportunity for startups and bio-entrepreneurs to gain personalized regulatory insights and accelerate their path to market.
The session is designed to support startups through focused one-on-one mentoring on regulatory pathways, compliance requirements, standards, quality management systems, and market readiness strategies.
Event Details :
Date : 26 May, 2026
Time : 10.30 AM - 1.30 PM
Mentoring Session : 30 minutes per startup
Seats : Limited, subject to screening
Participation is free, but seats are limited.
About the Mentors :
Chetna Dabi : Chetna works with the Regulatory Information and Facilitation Center (RIFC) at Venture Center and assists medical device startups in planning regulatory pathways, interpreting standards, and establishing and implementing quality management systems for medical devices. She is a certified Lead Auditor for ISO 9001 and ISO 13485 QMS.
Akash Dhade : Akash works with the Regulatory Information and Facilitation Center (RIFC) at Venture Center and assists organizations in identifying regulatory pathways, preparing technical documentation, and supporting submissions to notified bodies for the European market. He has over 10 years of experience in Quality Assurance and Regulatory Affairs (QARA), with specialization in EU, US, and Indian regulatory frameworks. He is also a Lead Auditor for ISO 13485 and ISO 9001.
For queries please contact
Aishwarya Varpe | +91 91564 65137 | aishwarya.varpe@venturecenter.co.in
Please Note :
Email invites along with the session joining link will be shared with shortlisted participants after screening of registration details.
