RQM+ is a global MedTech service provider focused on accelerating compliance and market success. Through our unparalleled expertise and industry knowledge, we deliver specialized solutions and expedite the journey along the full product lifecycle for Med Device and IVD companies, from concept to commercialization to post-market.

Our portfolio of services enables the delivery of end-to-end solutions across the complete med device product lifecycle, with our: 
• Regulatory and Quality Consulting
• Lab Services (Jordi Labs)
• Clinical Trials
• Reimbursement
• Technology Solutions


RQM+

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. 

Join 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 

*Certificate of attendance available upon request for live attendees.*
