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加拿大,强化对医疗器械上市后关于监督/风险管理的规定

JNM Global 제이엔엠글로벌 2021. 8. 17. 14:17

Health Canada医疗器械新型危险识别及评价管理的规定已变更
 

加拿大生部2018关于春季医疗器械上市后加强管和风险管理意进行了公示

因此,关于相应提案的2019615日在Canada Gazette, PartI进行了公示

 

以上延期至20206COVID

20201223日在Canada Gazette, Part II(CGII)公开

 

具体生效日期如下所示

据此,HC2021114布了4Updates指南,相Guidence如下所示

 

· Foreign risk notification for medical devices guidance document: Background

· Amendments to the Food and Drugs Act: Guide to new authorities

· Incident reporting for medical devices: Guidance document

· Guidance on summary reports and issue-related analyses for medical devices: Overview

 

https://www.canada.ca/en/health-canada/services/drugs-health-products/reports-publications/medeffect-canada/post-market-surveillance-medical-device-regulations-notice.html#a1


 

CMDR认证有什

可以通下方的们联系。

一定以最快的速度和最切的语气复您

 

info@china.net

info@jnmglobal.net