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X-ALT-DESC;FMTTYPE=text/html:<p style="text-align: justify;"><strong>What does it take to design clinical evidence that satisfies regulators and earns investor confidence ?&nbsp;</strong>A promising medical device innovation may open doors, but credible clinical evidence often determines whether it advances toward regulatory approval and investment readiness.&nbsp;</p>
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<p style="text-align: center;">As part of the Leap Global Bootcamp,&nbsp;<strong data-start="454" data-end="495"><span class="hover:entity-accent entity-underline inline cursor-pointer align-baseline"><span class="whitespace-normal">Venture Center</span></span></strong> will host a featured online talk on :</p>
<p style="text-align: center;"><strong data-start="532" data-end="617">Designing Clinical Evidence for Medical Devices: That Investors Actually Trust.</strong></p>
<p style="text-align: justify;"><strong>Organized by :&nbsp;</strong><span class="hover:entity-accent entity-underline inline cursor-pointer align-baseline"><span class="whitespace-normal">Leap Global Accelerator</span></span> and <span class="hover:entity-accent entity-underline inline cursor-pointer align-baseline"><span class="whitespace-normal">RIFC</span></span> @ Venture Center&nbsp;</p>
<p style="text-align: justify;"><strong>Supported by :&nbsp;</strong>DST NIDHI and Blockchain for Impact (BFI)&nbsp;</p>
<p style="text-align: justify;">The session is designed for <strong>founders, researchers, and innovators</strong> navigating the complex journey from device development to regulatory approval and investment readiness.</p>
<p style="text-align: justify;"><strong>Speaker Profiles : </strong></p>
<p style="text-align: justify;"><strong>Nikhil Khadabadi -&nbsp;</strong>Chief Medical Officer,&nbsp;<strong data-start="705" data-end="746"><span class="hover:entity-accent entity-underline inline cursor-pointer align-baseline"><span class="whitespace-normal">Eclevar MedTech</span></span></strong></p>
<ul style="list-style-type: square;">
<li style="text-align: justify;">Orthopaedic medical professional with strong expertise in medical devices, clinical research, and healthcare innovation</li>
<li style="text-align: justify;">Leads global clinical research initiatives, regulatory strategies, and post-market clinical follow-up (PMCF) activities at Eclevar MedTech</li>
<li style="text-align: justify;">Former Clinical Reviewer at <strong data-start="1045" data-end="1086"><span class="hover:entity-accent entity-underline inline cursor-pointer align-baseline"><span class="whitespace-normal">T&Uuml;V S&Uuml;D</span></span></strong>, with experience evaluating high-risk Class IIa, IIb, and III devices under EU MDD/MDR frameworks</li>
<li style="text-align: justify;">Orthopaedic specialist with expertise in clinical evaluation of prosthetic joints, spinal devices, and dental implants</li>
<li style="text-align: justify;">Clinical Lead at <strong data-start="1329" data-end="1370"><span class="hover:entity-accent entity-underline inline cursor-pointer align-baseline"><span class="whitespace-normal">Milo AI Healthcare</span></span></strong>, advancing AI-enabled clinical trials and medical decision-making</li>
</ul>
<p style="text-align: justify;"><strong data-start="0" data-end="16">Pierre Marie - </strong>Lead Medical Writer, Eclevar MedTech</p>
<ul style="list-style-type: square;">
<li style="text-align: justify;">Medical writer with <strong data-start="81" data-end="108">10+ years of experience</strong> supporting medical device and pharmaceutical companies in clinical and regulatory strategy.</li>
<li style="text-align: justify;">Expertise in <strong data-start="218" data-end="289">clinical evaluations, study design, and identifying regulatory gaps</strong> to strengthen market readiness.</li>
<li style="text-align: justify;">Develops scientific and regulatory documentation aligned with <strong data-start="388" data-end="431">EU MDR and MDCG international standards</strong>.</li>
<li style="text-align: justify;">Focuses on building <strong data-start="457" data-end="487">credible clinical evidence</strong> that supports both regulatory approvals and investor confidence.</li>
<li style="text-align: justify;">Experience across multiple therapeutic areas including <strong data-start="612" data-end="668">oncology, dermatology, wound care, and dental health</strong>.</li>
</ul>
<p style="text-align: justify;"><strong>What the talk will cover :&nbsp;</strong></p>
<ul style="list-style-type: square;">
<li style="text-align: justify;">What investors look for in a medical device evidence strategy</li>
<li style="text-align: justify;">The difference between regulatory minimum requirements and commercially credible evidence</li>
<li style="text-align: justify;">How intended use, claims, and device classification shape study design</li>
<li style="text-align: justify;">When literature evidence may be sufficient and when prospective clinical data becomes necessary</li>
<li style="text-align: justify;">Common evidence pitfalls that weaken fundraising conversations</li>
<li style="text-align: justify;">Building a staged clinical evidence roadmap aligned with company maturity and resources</li>
</ul>
<p style="text-align: justify;"><strong>Event Details :&nbsp;</strong></p>
<p style="text-align: justify;"><strong>Date :&nbsp;</strong>25th March, 2026&nbsp;</p>
<p style="text-align: justify;"><strong>Time :&nbsp;</strong>4.00 PM onwards&nbsp;</p>
<p style="text-align: justify;"><strong>Mode :&nbsp;</strong>Online via Zoom</p>
<p style="text-align: justify;"><strong><a class="btn btn-outline-primary" href="https://docs.google.com/forms/d/e/1FAIpQLSfU1flBEDVj0p-xJcUSVU-TY82TgQa2tuShxprceeZzkjpWtw/viewform">Register Here&nbsp;</a></strong></p>
<p style="text-align: justify;"><strong>For Queries Please Contact :&nbsp;</strong></p>
<p style="text-align: justify;">Aishwarya Varpe | +91 9156465137 | <a href="mailto:rifc@web.venturecenter.co.in">rifc@web.venturecenter.co.in</a>&nbsp;</p>
<p><strong><img style="display: block; margin-left: auto; margin-right: auto;" src="/storage/events/146/6d762cf3-4074-498b-be6b-6f47875ed937.png" width="1080" height="1350"></strong></p>
DESCRIPTION:What does it take to design clinical evidence that satisfies regulators and earns investor confidence ? A promising medical device innovation may open doors, but credible clinical evidence often determines whether it advances toward regulatory approval and investment readiness. 

As part of the Leap Global Bootcamp, Venture Center will host a featured online talk on :
Designing Clinical Evidence for Medical Devices: That Investors Actually Trust.
Organized by : Leap Globa...
LAST-MODIFIED:20260430T021923Z
LOCATION:Online via Zoom ...
SEQUENCE:0
STATUS:CONFIRMED
SUMMARY:Bringing a medical device to market requires more than a promising innovation. It requires the right clinical evidence strategy. This featured session will explore how startups can think about evidence generation in ways that strengthen both regulatory pathways and investor credibility.
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