Date: 13 November 2026
Time: 9:00am–10:00am (GMT+8)
For All GHWP members
As part of the GHWP Capacity Building program, we are pleased to announce an upcoming free webinar via Zoom on Speaking the Post-market surveillance based on systems, procedures, plans, and risk by Lane Ji, Director of Medical Business at DQS AP LTD. Lane Ji is also a senior lecturer, QMS auditor and Technical Documentation Reviewer at DQS MED Notified Body.
Post Market Surveillance is very important process to continually collect feedback and data from market and monitor device performance and safety. ISO has issued the standard - ISO/TR 20416:2020 Medical devices — Post-market surveillance for manufacturers, GHWP published the final document - Playbook for Design and Implementation of Active Post-Market Surveillance System in Dec 2025, China NMPA issued the Medical Device Vigilance Quality Management Specification in April 2026, EU enhanced PMS and PMCF requirement in MDR 2017/745.
This webinar provides a practical overview of the terminology, activities, deliverables, and regulatory expectations of Post Market Surveillance, and comparing the PMS requirements in different jurisdictions. Participants will learn what are active and passive Post-market surveillance, planning the PMS systems, procedures, plans and activities based on device type and risk analysis.
All are welcome to join with the Zoom access as follows:
Zoom Link: https://us06web.zoom.us/j/85856880813?pwd=rqRq23vp5yC80ABVG1taTIQXyzOSVe.1 Meeting ID: 858 5688 0813 Passcode: 540371 |
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Should you have any enquiry, please contact the GHWP Secretariat at secretariat@ghwp.org