Medical Device Competent Authorities 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 …

Overview - Public Health

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

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 …

Contacts - Public Health

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

European Committee for standardization (CEN) and European Committee for Electrotechnical Standardization (CENELEC) European Trade Federations Association …

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

To ease the process of finding drug and medical device regulators in Europe, Focus has updated its list of the website (s) for each country’s ministry of health …

Competent Authority, Notified Body, Authorized Representative

https://www.rimsys.io/blog/eu-competent-authority-notified-body-authorized-representative

According to EU directive 2017/745, it is a legal requirement to appoint a European Authorized Representative (EU Rep) for a medical device manufacturer who does not …

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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