Competent Authority Medical Devices Europe

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CAMD - Competent Authorities for Medical Devices : CAMD

https://www.camd-europe.eu/

In the context of the French Presidency of the EU Council, during its 50th plenary meeting, CAMD adopted a statement, following discussions about transition to MDR and capacity of the medical device system. CAMD recognise the significant and urgent challenges that …

Medical devices | European Medicines Agency

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

The Medical Devices Regulation applies since 26 May 2021. Manufacturers must comply with the Regulation when placing new medical devices on the market. It …

List of Competent Authorities for Medical Devices - AKRN

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

The competent authority belongs to the government of the Member State of the European Union (EU) and their responsibility is to transposes the requirements of …

National competent authorities (human) | European …

https://www.ema.europa.eu/en/partners-networks/eu-partners/eu-member-states/national-competent-authorities-human

List of national competent authorities in the EEA. Information on coronavirus …

Overview - Public Health

https://health.ec.europa.eu/medical-devices-dialogue-between-interested-parties/overview_en

The Essential List of Regulatory Authorities in Europe

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

Jan 22, 2020

Contacts - Public Health

https://health.ec.europa.eu/medical-devices-sector/new-regulations/contacts_en

European Federation of Precision Mechanical and Optical Industries (EUROM) European Industrial Federation committee on Medical Technology (EUROM VI) European …

EU Country Specific Medical Device Registration …

https://elsmar.com/elsmarqualityforum/threads/eu-country-specific-medical-device-registration-requirements.44865/

You may want to contact the competent authority of the each member state where the product is marketed (eg, Germany, Belgium, Italy, France). Normally, the …

EU Medical Device Vigilance Reporting in Europe - Emergo

https://www.emergobyul.com/services/medical-device-vigilance-and-incident-reporting-europe

The manufacturer or AR must notify the Competent Authorities (CA) of all affected countries, as well as the national CA where it is located, for any FSCA conducted in the …

List of national authorities for Medical Devices

https://easymedicaldevice.com/list-national-authorities-medical-devices/

Cyprus Medical Devices Competent Authority 1 Prodromou & 17 Chilonos Street, 1448 Nicosia, Cyprus Tel: +357 22605572/735 – Fax: +357 22468427 e-mail: …

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