Europe – 38ème organisme notifié au titre du Règlement 2017/745 

38ème organisme notifié au titre du Règlement 2017/745 
As coronavirus roils region, EU device body adamant about steps to hit MDR deadline

Europe – Le règlement (UE) 2023/607

Le règlement (UE) 2023/607, publié au JOUE, modifie les dispositions transitoires relatives à certains dispositifs médicaux et à certains dispositifs médicaux de diagnostic in...

Europe – Publication of the Third Edition of the “Clinical Evidence Requirements under EU...

We are pleased to announce the publication of the Third Edition of the “Clinical Evidence Requirements under EU In Vitro Diagnostics Regulation” Regulatory eBook. The Questions and Answers eBook was developed by...
Joint Implementation/preparedness plan on the new Medical Devices Regulation 2017/745 (MDR) on March 11th, 2020

Europe – European Regulators Move to Increase Notified Body Capacity

The European Commission (EC) has taken new measures to relieve some of the pressure on Notified Bodies and free up capacity to perform medical...

Europe – Advisory group urges UK to ‘rapidly explore’ recognition of US device approvals

A group formed to advise the UK government on the regulation of medical devices is pushing for officials to “rapidly explore” building an equivalence...
Joint Implementation/preparedness plan on the new Medical Devices Regulation 2017/745 (MDR) on March 11th, 2020

Europe – Council votes unanimously to extend MDR deadlines

The European Council (EC) has approved a measure to extend the transition period for medical devices under the Medical Devices Regulation (MDR) and to...
MHRA Offers Grace Period for Device Manufacturers Dealing With Withdrawn Notified Bodies

UK – Impact of extension of Medical Device Regulations transitional period and the validity...

The EU is introducing more time to certify certain medical devices under EU Medical Device Regulation (“EU MDR”). The proposal recognises the challenges in capacity across...

Europe – La prolongation de la période de transition pour les dispositifs médicaux et...

L’amendement qui modifie les Règlements (UE) 2017/745 et (UE) 2017/746 en ce qui concerne les dispositions transitoires relatives à certains dispositifs médicaux (DM) et...

Europe – Nouvel Organisme Notifié au titre du règlement (UE)2017/746

Nouvel Organisme Notifié au titre du règlement (UE)2017/746 : MDC MEDICAL DEVICE CERTIFICATION GMBH...

Europe – Nouvel Organisme Notifié au titre du règlement (UE)2017/746

Nouvel Organisme Notifié au titre du règlement (UE)2017/746 : National Standards Authority of Ireland (NSAI)...

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