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MDCG 2020-12 Transitional provisions for consultations of authorities on devices incorporating a substance which may be considered a medicinal product [...] as well as on devices manufactured using TSE susceptible animal tissues
Document date: Tue Jun 09 00:00:00 CEST 2020
- Created by GROW.R.2.DIR
- Publication date: n/a
- Last update: Wed Jun 10 14:20:09 CEST 2020
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MDR and IVDR implementing measures rolling plan
Document date: Tue Jun 02 00:00:00 CEST 2020
- Created by GROW.R.2.DIR
- Publication date: n/a
- Last update: Wed Jun 03 14:35:39 CEST 2020
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Planned meetings of Medical Device Coordination Group (MDCG) and subgroups in 2020
Document date: Thu May 28 00:00:00 CEST 2020
- Created by GROW.R.2.DIR
- Publication date: n/a
- Last update: Tue Jun 02 07:10:32 CEST 2020
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MDCG 2020-11 Guidance on the renewal of designation and monitoring of notified bodies under Directives 90/385/EEC and 93/42/EEC to be performed in accordance with Commission Implementing Regulation (EU) 2020/666 amending Commission Implementing Regulatio
Document date: Wed May 27 00:00:00 CEST 2020
- Created by GROW.R.2.DIR
- Publication date: n/a
- Last update: Thu May 28 07:11:03 CEST 2020
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Amendment to Implementing Regulation 920/2013 on the designation of notified bodies
Document date: Mon May 25 00:00:00 CEST 2020
- Created by GROW.R.2.DIR
- Publication date: n/a
- Last update: Tue May 26 11:10:31 CEST 2020
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