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EMA issues presentation on the pilot for expert panels for high-risk medical devices |

https://www.ema.europa.eu/en/documents/presentation/presentation-information-session-pilot-expert-panels-scientific-advice-manufacturers-certain-high_en.pdf

News

23 Aug
EU Commission issues decision flowchart for devices covered by the MDR transitional period |
16 Aug
EU Commission issues guidance on the summary of the clinical study report |
15 Aug
CEO presentation on Adverse Events handling under the MDR (2017/745) |
10 Jul
EU Commission adopts decision for safe EU-US data flows |
12 May
MDCG updates guidance on significant changes for MDD and AIMDD devices |
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