REGISTRATION | One-on-one mentoring| Regulatory requirements for medical device startups for Indian, European and US markets | 27 Feb 2026 | 10:30 AM to 1:30 PM | Hybrid Mode
Wish to take your medtech startup product to the Indian, USA or European markets?
Consult our regulatory expert to get his guidance for country specific medical device regulations.

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 assisted 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.

The mentoring session is free, but registration is mandatory!
 
NOTE: Details will be emailed to shortlisted participants post-screening of registration details. 
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Name *
Email ID
 *
Contact number *
Name of your Startup/Organization
 *
Please mention the city where your startup is based
 *
Product Name *
Specify the intended use of your medical device *
At which stage is you product?
(e.g. D&D, Prototyping, Testing, Clinical Trial , Manufacturing)
 *
Is your device commercialized in any global market? If yes please specify? 
If no please mention NA
 *
Please mention which particular regulatory requirement consultation are you looking for from our regulatory expert. *
Specific questions/ points to discuss with the experts. 
(NOTE: Shortlisting process post registration will also be based on the kind of questions for discussion. Thus, kindly be specific while writing the points for discussion with the expert)
 *
Mode of Attending *
How did you get to know about this event? *
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