R-Clinic for Medical Device Startups provides strategic regulatory guidance to bridge the gap between innovation and market readiness. This specialized RIFC program at Venture Center offers comprehensive expertise across critical compliance areas including ISO 13485 Quality Management Systems, advanced labelling and packaging standards, cybersecurity protocols, and Software as Medical Device (SaMD) frameworks. The initiative empowers MedTech entrepreneurs to navigate complex regulatory landscapes with precision and clarity, transforming compliance challenges into strategic advantages for faster market entry.
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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.
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Email Invites along with session joining link will be sent to shortlisted participants post screening of registration details
For More Information Contact:
Aishwarya Varpe | aishwarya.varpe@venturecenter.co.in | +91-9156465137