CDR Workshop on Techniques for Medical Device Adverse Events Monitoring
Date: 23 - 24 April
Organizer: Center for Drug Re-evaluation
Price: RMB 1,200 per participant, including fees for training and material
Venue: Wuxi City, Jiangsu province.
Deadline for registration: 10th April
Dear WG Members:
The Center for Drug Re-evaluation will hold a 2 days workshop on Techniques for Medical Device Adverse Events Monitoring from 23rd to 24th of April. The goal is to To fully promote the understanding of all the requirements stipulated in the Measure for medical device manufacturers, distributors, and user facilities, and to help them develop skills on promptly and efficiently monitoring and re-evaluating medical devices in the market.
Attached below the invitation in both Englishand Chinese, including the detailed content, contact person and registration form. For further detailed information towards this workshop, you may contact directly with the organizer.
To having an overview on Position of EUCCC-Eucomed-COCIR towards this issue, please also find the Consolitated Comments and its Cover letter submitting to SFDAon "Interim Measure on Medical Device Adverse Events (AE) Monitoring and Re-Evaluation" attached below in this email.
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For any further information about the Healthcare Equipment Working Group, general inquiries such as Membership with the European Chamber or our partner associations, please contact Ms. Yujie Bao (for COCIR) at ybao@euccc.com.cn or Ms. Penny Zhao (for Eucomed) at yzhao@euccc.com.cn.