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BEGIN:VEVENT
DTSTART:20260630T050000Z
DTEND:20260630T080000Z
DTSTAMP:20260626T012102Z
UID:737b6e98-e58c-4052-b0cb-0b3ca3b5f805
CREATED:20260624T090800Z
X-ALT-DESC;FMTTYPE=text/html:<h6 style="text-align: center;">Building a Medical Device, SaMD, or IVD startup? Get personalized regulatory insights from certified experts and accelerate your path to market &mdash; one focused 30-minute session at a time.</h6>
<h3 style="text-align: center;"><strong>R-Clinic for Startups</strong></h3>
<p style="text-align: center;"><span style="background-color: rgb(194, 224, 244);"><strong><em>A focused regulatory mentoring session for startups developing Medical Devices, SaMD, or IVDs</em></strong></span></p>
<h6 style="text-align: justify;"><strong>Event Details:</strong></h6>
<ul>
<li style="text-align: justify;"><strong>Date:</strong> Tuesday, 30th June 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> 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. Email invites along with the session joining link will be sent to shortlisted participants post-screening of registration details.</p>
<p style="text-align: justify;"><a class="btn btn-outline-primary" href="https://forms.gle/X4dmVvnWcPcgwLAL6"><strong>Register Now&nbsp;</strong></a></p>
<h6 style="text-align: justify;"><strong>About the Mentors:</strong></h6>
<p style="text-align: justify;"><a href="http://linkedin.com/in/chetna-dharmavat-dabi-bb0598197"><strong>Chetna Dabi</strong></a> 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. <a href="http://linkedin.com/in/chetna-dharmavat-dabi-bb0598197" target="_blank" rel="noopener">More about Chetna</a></p>
<p style="text-align: justify;"><a href="http://linkedin.com/in/connect-akash-dhade"><strong>Akash Dhade</strong></a> 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 notified bodies for the European market. He has 10+ years of experience in QARA, with specialization in EU, US, and India regulations, and is a certified Lead Auditor for ISO 13485 and ISO 9001.&nbsp;</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><img style="display: block; margin-left: auto; margin-right: auto;" src="/storage/events/169/9e3df57d-d0dd-42ce-922d-26b7ebdbdffc.png" alt="" width="500" height="647"></p>
DESCRIPTION:Building a Medical Device, SaMD, or IVD startup? Get personalized regulatory insights from certified experts and accelerate your path to market — one focused 30-minute session at a time.
R-Clinic for Startups
A focused regulatory mentoring session for startups developing Medical Devices, SaMD, or IVDs
Event Details:

Date: Tuesday, 30th June 2026
Time: 10.30 AM – 1.30 PM
Format: 30-minute mentoring session per startup (Limited Seats)
Mode: Online via Google Meet

Participat...
LAST-MODIFIED:20260626T012102Z
LOCATION:Hybrid...
SEQUENCE:0
STATUS:CONFIRMED
SUMMARY:R-Clinic for Startups developing Medical Devices, SaMD, or IVDs, a unique opportunity to gain personalized regulatory insights and accelerate your path to market.
TRANSP:OPAQUE
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