European Regulatory Authority Medical Devices

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Medical devices | European Medicines Agency

https://www.ema.europa.eu/en/human-regulatory/overview/medical-devices

The Regulations on Medical Devices (Regulation (EU) 2017/745) and on In Vitro Diagnostic Devices (Regulation (EU) 2017/746) changed the European legal framework for medical devices, introducing new responsibilities for EMA and national …

Medical Device Regulation comes into application

https://www.ema.europa.eu/en/news/medical-device-regulation-comes-application

Medical Device Regulation comes into application. Regulation (EU) 2017/745 on medical devices becomes applicable in the European Union today, 26 May …

Medical Devices - New regulations - Public Health

https://health.ec.europa.eu/medical-devices-new-regulations_en

Medical Devices - New regulations Overview The EU has revised the legal framework of 3 directives to reflect progress over the last 20 years. Getting ready …

Medical Devices - Sector - Public Health

https://health.ec.europa.eu/medical-devices-sector_en

The following medical devices Directives were repealed and replaced by Regulation (EU) 2017/746 and Regulation (EU) 2017/745 respectively... New …

The Essential List of Regulatory Authorities …

https://www.raps.org/news-and-articles/news-articles/2020/1/the-essential-list-of-regulatory-authorities-in-eu

Jan 22, 2020

The European Union Medical Device Regulation – …

https://eumdr.com/

Press release 26 May 2021: announcing Stronger rules on medical devices (EU MDR) have entered into application. Publication of MDCG 2021-8 Clinical investigation …

List of Competent Authorities for Medical Devices - AKRN

https://akrnconsulting.com/list-member-states-competent-authorities-for-medical-devices/

In the case of medical devices, Article 101 of Regulation (EU) 2017/745 on Medical Devices (MDR) indicates that each Member States shall designate a competent …

European Medicines Agency

https://www.ema.europa.eu/en

Public consultation on a multi-stakeholder platform to improve clinical trials in the EU On 3 February 2023, EMA, the Heads of Medicines Agencies (HMA) and the European …

New European MDCG Guidance on Medical Device Vigilance …

https://www.emergobyul.com/news/new-european-mdcg-guidance-medical-device-vigilance-requirements

The long-awaited Medical Device Coordination Group (MDCG) Guidance on Vigilance has been published to the European Commission website. MDCG 2023-3, …

European Medical Device Regulation | Deloitte Netherlands

https://www2.deloitte.com/nl/nl/pages/risk/articles/european-medical-device-regulation.html

The complexity of qualification and classification. The European Medical Device Regulation 2017/745 (EU-MDR) provides a regulatory framework with the purpose of …

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