National Competent Authorities Medical Devices

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 of the European Self-Medication Industry (AESGP) European Coordination of the …

Overview - Public Health

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

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 …

Medical Devices: Post Market Surveillance National …

https://www.imdrf.org/sites/default/files/2022-05/IMDRF%20NCAR%20WG%20N14Final%202022.pdf

Reportable events, associated with a medical device that have led or are highly likely to lead to unanticipated serious public health threat and fulfill the following criteria: Death of …

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: …

Medical Devices: Post-Market Surveillance: National …

https://www.imdrf.org/documents/medical-devices-post-market-surveillance-national-competent-authority-report-exchange-criteria-and-report-form

Medical Devices: Post-Market Surveillance: National Competent Authority Report Exchange Criteria and Report Form | International Medical Device …

Competent Authority, Notified Body, Authorized Representative

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

There is an umbrella group called the Competent Authorities for Medical Devices that is ...

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 …

Országos Gyógyszerészeti és Élelmezés-egészségügyi Intézet

https://ogyei.gov.hu/medical_devices/

From 26 May 2021, economic operators placing class I medical devices on the market must be in compliance with Regulation (EU) 2017/745 on medical devices …