欧盟医疗器械MDR法规上市后监管体系

加强器械上市后监管体系
Chapter VIIPOST-MARKET SURVEILLANCE, VIGILANCE AND MARKETSURVEILLANCE 着重说明上市后监管、警戒和市场监管。
1.建立、实施和维护上市后监管体系（见Article83）。
2.强调上市后监管体系贯穿整个生命周期，并不断更新。
3.建立“上市后监管计划”（见Article84），具体内容见Annex III。
4.I类器械编写“上市后监管报告”（见Article85）。
5.IIa、IIb和III类器械编制“定期安全性更新报告（PSUR）”（见Article86）。
6.PSUR需定期更新并作为技术文件的一部分。
7. 建立警戒和上市后监管电子系统（见Article92）。
8. 在整个器械使用寿命期间，依据实施PMCF后取得的临床数据对临床评价及技术文件进行更新（Annex XIV partB）。

Strengthen the post market supervision system of devices

Chapter VIIPOST-MARKET SURVEILLANCE, VIGILANCE AND MARKETSURVEILLANCE emphasize post listing supervision, vigilance andmarket supervision.

1. Establish, implement and maintain the post listing regulatorysystem (see Article 83).

2. Emphasize that the post listing regulatory system runsthrough the entire life cycle and is constantly updated.

3. Establish a "post listing supervision plan" (see Article 84),and see Annex III for details.

4. Class I devices shall prepare a "post marketing regulatoryreport" (see Article 85).

5. Class IIa, IIb and III devices prepare "Periodic SafetyUpdate Report (PSUR)" (see Article 86).

6. PSUR shall be updated regularly and taken as a part oftechnical documents.

7. Establish an electronic system for alert and post marketingsupervision (see Article 92).

8. During the whole service life of the device, update theclinical evaluation and technical documents according to theclinical data obtained after the implementation of PMCF (Annex XIVpart B).