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Loi Bertrand
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FDA

6 days ago
2 min

MDR :A summary of key features to help you complying with language and translation requirements 6/6

Sep 17
2 min

MDR: The marketing and post-market surveillance phases (5/6)

May 25
1 min

Connected Medical Devices To Necessitate Clinical Evaluation Requires MDR

May 4
1 min

The European Commission's guide on medical devices in the Covid-19 context

Apr 17
2 min

MDR or not MDR, that is the question... Not any longer

Feb 27
3 min

MDR: The Registration Phase (4/6)

Feb 12
2 min

MDR: The Pre-registration Phase (3/6)

Jan 30
1 min

Of MDR and Translations (2/6)

Jan 16
1 min

THE EU MEDICAL DEVICE REGULATION 2017 /745 : A new opportunity to be ready in time (1/6)

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