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BEGIN:VEVENT
DTSTART:20250422T053000Z
DTEND:20250422T063000Z
DTSTAMP:20260430T123300Z
UID:261b762f-2548-438b-8cdb-496af5be496a
CREATED:20250411T064900Z
X-ALT-DESC;FMTTYPE=text/html:<h6><span style="font-size: 16pt;"><strong><a href="/services/advisory-and-consulting/regulatory-information-and-facilitation">Regulatory Information and Facilitation</a> is happy to announce an Awareness Talk on the FDA&rsquo;s Quality Management System Regulation (QMSR) Final Rule for medical device manufacturers.</strong></span></h6>
<hr>
<p><strong>What to expect:</strong></p>
<ul>
<li>Introduction to QMSR and its purpose</li>
<li>Differences between 21 CFR Part 820 and ISO 13485</li>
<li>Compliance timeline and transition strategy</li>
<li>Impact on medical device manufacturers</li>
<li>Best practices for QMS alignment</li>
<li>Live Q&amp;A with the expert</li>
</ul>
<p><strong>Date: </strong>22 April 2025<br><strong>Time: </strong>11:00 AM &ndash; 12:00 PM IST<br><strong>Mode: </strong>Zoom (Online)</p>
<p><strong>Speaker:&nbsp;</strong><a href="https://www.linkedin.com/in/connect-akash-dhade/">Akash Dhade</a> (Associate Manager &ndash; Regulatory Services)</p>
<p><a class="btn btn-outline-primary" href="https://forms.gle/JEc4LCdrQTBnUR4KA">Register Now</a><br><em><span style="font-size: 10pt;">(Email invites along with a session joining link will be sent one day before the event.)</span></em></p>
<p>For more information contact: Aishwarya Varpe | aishwarya.varpe@venturecenter.co.in | <a href="tel:9156465137">9156465137</a></p>
<p><img style="display: block; margin-left: auto; margin-right: auto;" src="/storage/events/72/8cc7f82f-f1af-4d60-b444-a8d508b2e71f.png" alt="" width="500" height="419"></p>
DESCRIPTION:Regulatory Information and Facilitation is happy to announce an Awareness Talk on the FDA’s Quality Management System Regulation (QMSR) Final Rule for medical device manufacturers.

What to expect:

Introduction to QMSR and its purpose
Differences between 21 CFR Part 820 and ISO 13485
Compliance timeline and transition strategy
Impact on medical device manufacturers
Best practices for QMS alignment
Live Q&A with the expert

Date: 22 April 2025Time: 11:00 AM – 12:00 PM ...
LAST-MODIFIED:20260430T123300Z
LOCATION:Hybrid...
SEQUENCE:0
STATUS:CONFIRMED
SUMMARY:Awareness Talk on the FDA’s Quality Management System Regulation (QMSR) Final Rule for medical device manufacturers.
TRANSP:OPAQUE
END:VEVENT
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