New Guidance Templates for the Post-Market Clinical Follow-Up (PMCF) Plan and PMCF Evaluation Report
Author: Suzanne Broussard The newest guidance documents for post-market clinical follow-up (PMCF) requirements have just been released by the Medical Device Coordination Group (MDCG). The two documents provide guidance templates for the PMCF plan and the […]
[FREE WEBINAR] Live Q&A Follow-Up: How to Assess Your CER for MDR Readiness, Part 1
Click here to watch the recording. We had such a large turnout at our previous webinar, How to Assess Your CER for MDR Readiness, Part 1, and left with some […]
The Summary of Safety and Clinical Performance (SSCP) Provides Valuable Information to Health Care Providers, Patients, and Manufacturers
Author: Suzanne Broussard Is your organization ready to display to the world your medical devices safety and performance record? The Summary of Safety and Clinical Performance (SSCP) is one of the new requirements imposed by manufacturers by […]
