《 MDCG 2020-7 Guidance on PMCF Plan Template(2022-5-20)》电子宣传画册作品由SGS中国于2022-5-20制作并发布于云展网电子画册制作平台。云展网是电子画册,企业宣传册,期刊杂志在线制作平台,一键上传PDF即转为逼真的3D翻页画册,或直接套用模板,生成永久有效的链接/二维码,微信扫码即可分享。 说明手册 产品...
Medical Device n Group Document MDCG 2020-7 n The Medical Device n Group (MDCG) has released the MDCG 2020-7 document。which provides guidance on post-market clinical follow-up plans for medical devices。This document is XXX (IVDR). Post-Market Clinical Follow-Up Plan Template The MDCG ...
1 Ref. Ares(2020)2214397 - 24/04/2020 Medical Device Medical Device Coordination Group Document MDCG 2020-7 This document has been endorsed by the Medical Device Coordination Group (MDCG) established by Article 103 of Regulation (EU) 2017/745. The MDCG is composed of representatives of all...
2020年11月2日 2020年4月,欧盟委员会(EC)公布了医疗器械协调小组(MDCG) MDCG 2020-7 Post-market clinical follow-up (PMCF) Plan Template 和MDCG 2020-8 Post-market clinical follow-up (PMCF) Evaluation R…
MDCG 2020-7 上市后临床随访 (PMCF) 计划模板中文版.docx,医疗疗 医疗疗器械 医疗器械协调组织文件 MDCG 2020-7 MDCG 2020-7 MDCG 2020-7 上市后临床随访 (PMCF) 计划模板制造商和公告机构指南 2020 年 4 月 本文件已得到根据法规 (EU) 第 103 条设立的医疗器械协调组 (MDCG
内容提示: MDCG 2020-7 Post-market clinical follow-up (PMCF) Plan Template A guide for manufacturers and notified bodies 上市后临床跟踪(PMCF )计划模板 给制造商和公告机构的指南 April 2020 2020 年年 04 月 This document has been endorsed by the Medical Device Coordination Group (MDCG) ...
Medical Device Coordination Group Document MDCG 2020-7 5 Post-market clinical follow-up plan Template PMCF plan number: PMCF plan date: PMCF plan version: Revision history Rev Revision date Description of change Revised by Section A. Manufacturer contact details ...
MDCG 2020-7 上市后临床随访计划模板 PMCF Plan Template.pdf,Ref. Ares(2020)2214397 - 24/04/2020 Medical Device Medical Device Coordination Group Document MDCG 2020-7 MDCG 2020-7 Post-market clinical follow-up (PMCF) Plan Template A guide for manufacturers
MDCG 2020-7_guidance_pmcf_plan_template_en
MDCG 2020-7 PMCF计划模板Ref. Ares(2020)2214397 - 24/04/2020 Medical Device CoordinationGroupDocumentMDCG2020-7 ThisdocumenthasbeenendorsedbytheMedicalDeviceCoordinationGroup(MDCG)establishedbyArticle103ofRegulation(EU) 2017/745. The MDCG is composed of representatives of all Member States and it is...