BEGIN:VCALENDAR
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BEGIN:VEVENT
DTSTART:20261030T050000Z
DTEND:20261030T080000Z
DTSTAMP:20261007T212940Z
UID:ec0e5e8d-b6db-47bf-8783-cd45f19ec43b
CREATED:20261005T085500Z
X-ALT-DESC;FMTTYPE=text/html:<h6 style="text-align: center;">Developing a Medical Device, SaMD, or IVD? Discuss your regulatory questions with an expert in a focused, one-on-one mentoring session.</h6>
<h3 style="text-align: center;"><strong>Regulatory Requirements for MedTech Startups</strong></h3>
<p style="text-align: center;"><span style="background-color: rgb(194, 224, 244);"><strong><em>Free one-on-one mentoring | 30 minutes per startup | Limited seats</em></strong></span></p>
<h6 style="text-align: justify;"><strong><img src="/storage/events/189/52135a10-7888-4ace-ac3e-729f36c8b097.png" alt="" width="1545" height="1999"></strong></h6>
<h6 style="text-align: justify;"><strong>Event Details:</strong></h6>
<ul>
<li style="text-align: justify;"><strong>Date:</strong> 30th October 2026</li>
<li style="text-align: justify;"><strong>Time:</strong> 10:30 AM &ndash; 1:30 PM</li>
<li style="text-align: justify;"><strong>Format:</strong> One-on-one, 30-minute mentoring session per startup <em>(Limited Seats)</em></li>
<li style="text-align: justify;"><strong>Mode:</strong> Online via <strong>Google Meet</strong></li>
</ul>
<p style="text-align: justify;">Participation is free; however, prior registration is mandatory. Register to book your slot and discuss the regulatory requirements relevant to your startup.</p>
<p style="text-align: justify;"><a class="btn btn-outline-primary" href="https://forms.gle/X4dmVvnWcPcgwLAL6" target="_blank" rel="noopener"><strong>Register Now</strong></a></p>
<h6 style="text-align: justify;"><strong>Topics for Discussion:</strong></h6>
<ul>
<li style="text-align: justify;">Planning regulatory pathways for India, the USA, and the EU</li>
<li style="text-align: justify;">Health Insurance Portability and Accountability Act (HIPAA)</li>
<li style="text-align: justify;">Digital Personal Data Protection (DPDP) Act advisory</li>
<li style="text-align: justify;">ISO 27001 Information Security Management System</li>
<li style="text-align: justify;">ISO 13485 Quality Management Standard</li>
<li style="text-align: justify;">Identification of applicable standards</li>
<li style="text-align: justify;">ISO 9001 Quality Management Standard</li>
<li style="text-align: justify;">Risk management</li>
<li style="text-align: justify;">Clinical trial advice</li>
</ul>
<h6 style="text-align: justify;"><strong>About the Mentor:</strong></h6>
<p style="text-align: justify;"><a href="https://www.linkedin.com/in/chetna-dharmavat-dabi-bb0598197" target="_blank" rel="noopener"><strong>Chetna Dabi</strong></a> 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. <a href="https://www.linkedin.com/in/chetna-dharmavat-dabi-bb0598197" target="_blank" rel="noopener">More about Chetna</a></p>
<p style="text-align: justify;"><strong>For queries please reach out to:</strong></p>
<p style="text-align: justify;">Aishwarya Varpe | +91 91564 65137 | <a href="mailto:aishwarya.varpe@venturecenter.co.in">aishwarya.varpe@venturecenter.co.in</a></p>
<p>&nbsp;</p>
DESCRIPTION: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...
LAST-MODIFIED:20261007T212940Z
LOCATION:Online (Google Meet)...
SEQUENCE:0
STATUS:CONFIRMED
SUMMARY:Venture Center’s Regulatory Information and Facilitation Center (RIFC) is offering free, one-on-one mentoring for startups developing Medical Devices, SaMDs, and IVDs. Discuss your questions with Chetna Dabi, Associate Manager, Regulatory Services, on regulatory pathways, applicable standards, quality management, data protection, risk management, and clinical trials.
TRANSP:OPAQUE
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