<p><em>This panel was recorded October 2, 2025.⁠⁠⁠⁠ We hope you&#39;ll join us live in the future to ask your own questions and participate in the attendee chat! See similar events on demand and read other free MedTech resources at </em><a href="https://www.rqmplus.com/resources/">⁠⁠<em>RQMplus.com</em>⁠⁠</a><em>.</em></p><p><br></p><p>PMCF surveys can strengthen your CER and PSUR or create rework. In this 60-minute panel with live audience Q&amp;A, RQM+ leaders from regulatory, clinical, and scientific writing share what MDR reviewers look for and how to design surveys that generate decision-grade evidence. The session is intended for regulatory affairs, post-market surveillance, clinical evidence, and medical writing leaders at MedTech manufacturers.</p><p><br></p><p>Listen to learn how to: </p><ul><li>Define clear objectives, endpoints, and target population so the survey maps to your PMCF plan and CER. </li><li>Improve response rates without bias and capture higher-quality data, including adverse events and usability feedback. </li><li>Learn how to position your physician level survey as a chart review. </li><li>Document methods, rationales, and traceability so notified bodies can follow the logic. </li><li>Avoid the top reasons reviewers push back on PMCF surveys and how to correct them. </li></ul><p><br></p><p>Walk away with a practical checklist to pressure test your next PMCF survey and reduce review risk. </p><p><br></p><p>Who should attend: </p><ul><li>Regulatory affairs leaders and PMS managers. </li><li>Clinical evidence and clinical operations leads. </li><li>Scientific and medical writing leaders, including CER and PSUR authors. </li><li>Quality leaders responsible for post market surveillance programs. </li></ul><p><br></p><p>Panelists and moderator: </p><ul><li>Torrie DeGennaro – Vice President, Scientific &amp; Medical Writing </li><li>Bethany Chung, Ph.D., RAC – Director, Technical Solutions &amp; Innovation </li><li>Garrett Jeffries, Ph.D. – Principal </li><li>Jon Gimbel, Ph.D. – Vice President, Regulatory Affairs</li></ul><p><br></p><p>--</p><p>📲<a href="https://www.linkedin.com/company/rqmplus/">⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Follow RQM+ on LinkedIn.⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠</a></p><p>💼<a href="https://www.rqmplus.com/careers#open-positions">⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Check out our open positions.⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠</a></p><p>📚<a href="https://www.rqmplus.com/expert-content">⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠See free on-demand content.⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠</a></p><p>📝 If you&#39;d like to speak with us directly about how we might be able to support you and your organization, you&#39;re welcome to use <a href="https://www.rqmplus.com/book-consultation">⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠our contact form⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠</a>.</p>