This panel was recorded October 2, 2025.⁠⁠⁠⁠ We hope you'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 ⁠⁠RQMplus.com⁠⁠.

PMCF surveys can strengthen your CER and PSUR or create rework. In this 60-minute panel with live audience Q&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.

Listen to learn how to:

Define clear objectives, endpoints, and target population so the survey maps to your PMCF plan and CER.
Improve response rates without bias and capture higher-quality data, including adverse events and usability feedback.
Learn how to position your physician level survey as a chart review.
Document methods, rationales, and traceability so notified bodies can follow the logic.
Avoid the top reasons reviewers push back on PMCF surveys and how to correct them.

Walk away with a practical checklist to pressure test your next PMCF survey and reduce review risk.

Who should attend:

Regulatory affairs leaders and PMS managers.
Clinical evidence and clinical operations leads.
Scientific and medical writing leaders, including CER and PSUR authors.
Quality leaders responsible for post market surveillance programs.

Panelists and moderator:

Torrie DeGennaro – Vice President, Scientific & Medical Writing
Bethany Chung, Ph.D., RAC – Director, Technical Solutions & Innovation
Garrett Jeffries, Ph.D. – Principal
Jon Gimbel, Ph.D. – Vice President, Regulatory Affairs

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