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Brexit: What is the impact of the TCA on EU-UK Medical Device regulations?

Jan 7, 20214 min read

Brexit: What is the impact of the TCA on EU-UK Medical Device regulations?

MDR: key features to comply with language and translation requirements 6/6

Nov 26, 20202 min read

MDR: key features to comply with language and translation requirements 6/6

Les dispositifs médicaux et la FDA (3/3) : les alternatives à la 510(k) traditionnelle et à la APM

Nov 19, 20203 min read

Les dispositifs médicaux et la FDA (3/3) : les alternatives à la 510(k) traditionnelle et à la APM

Les dispositifs médicaux et la FDA (2/3) : GMPs/QSRs et ISO 13485

Nov 12, 20203 min read

Les dispositifs médicaux et la FDA (2/3) : GMPs/QSRs et ISO 13485

Les dispositifs médicaux et la FDA (1/3)

Oct 26, 20204 min read

Les dispositifs médicaux et la FDA (1/3)

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

Sep 17, 20202 min read

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

Connected Medical Devices To Necessitate Clinical Evaluation Requires MDR

May 25, 20201 min read

Connected Medical Devices To Necessitate Clinical Evaluation Requires MDR

Advertising your Medical Device in France: Use of Allegations and Comparisons

May 19, 20202 min read

Advertising your Medical Device in France: Use of Allegations and Comparisons

May 5, 20201 min read

Advertising your medical device in France during the state of health emergency

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

May 4, 20201 min read

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

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