Developing a Medical Device, SaMD, or IVD? Discuss your regulatory questions with an expert in a focused, one-on-one mentoring session.
Regulatory Requirements for MedTech Startups
Free one-on-one mentoring | 30 minutes per startup | Limited seats
Event Details:
- Date: 30th October 2026
- Time: 10:30 AM – 1:30 PM
- Format: One-on-one, 30-minute mentoring session per startup (Limited Seats)
- Mode: Online via Google Meet
Participation is free; however, prior registration is mandatory. Register to book your slot and discuss the regulatory requirements relevant to your startup.
Topics for Discussion:
- Planning regulatory pathways for India, the USA, and the EU
- Health Insurance Portability and Accountability Act (HIPAA)
- Digital Personal Data Protection (DPDP) Act advisory
- ISO 27001 Information Security Management System
- ISO 13485 Quality Management Standard
- Identification of applicable standards
- ISO 9001 Quality Management Standard
- Risk management
- Clinical trial advice
About the Mentor:
Chetna Dabi is Associate Manager, Regulatory Services, at the Regulatory Information and Facilitation Center (RIFC), Venture Center. She assists medical device startups in planning regulatory pathways, interpreting standards, and establishing and implementing quality management systems. She is a certified lead auditor for ISO 9001 and ISO 13485. More about Chetna
For queries please reach out to:
Aishwarya Varpe | +91 91564 65137 | aishwarya.varpe@venturecenter.co.in