Time: 19 November 2025, 9.30am-10.30am(GMT +8)
For All GHWP members
As part of the GHWP Capacity Building program, we are pleased to announce an upcoming free online training via Zoom on “Medical Device Post Market Surveillance”. This session will feature experts from Industry.
This session is organized and delivered by WG4. It is designed to share best practices in enhancing post-market complaint processing through AI workflow implementation. Additionally, we will provide updates on the EU MDR Post-Market Surveillance (PMS) requirements.
The training will serve as a collaborative platform for discussion, knowledge exchange, and sharing of implementation experiences. It aims to foster dialogue and encourage the adoption of effective and innovative practices across teams.
No registration is required for this online training. Target audiences, regulators and industry who are interested, are welcome to join with the Zoom access as follows:
Zoom link: https://us06web.zoom.us/j/89137339297?pwd=9HZUtwlKfJJ2ufjSPax5NDK2DicyKO.1 Meeting ID: 891 3733 9297 Passcode: 579569 |
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Should you have any enquiry, please contact the GHWP Secretariat at secretariat@ghwp.info
| Time | Topic | Speaker |
|---|---|---|
| 9:30-9:35am | Opening remark | Dr. Aaron Hung WG4 Acting Chair
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| 9:35-10:00pm | Enhancing Post-Market Complaint Processing-AI Workflow Implementation | Dr. Nick Currlin
Medical Director, Medical Device Safety AbbVie |
| 10.00-10:25am | EU MDR Post Market Surveillance | Ms. Ashe Archana
Regulatory Affairs Director, Global Post Market CoE GE HealthCare
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| 10.25-10:30am | Closing remark | Ms. Kitty Mao WG4 Co-chair
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