FAQ Regulation MD - Notified bodies

Name: FAQ Regulation MD - Notified bodies
Creator: National Agency for the Safety of Medicines and Health Products
Keywords: applications,faq,frequently-asked-questions,notified-bodies,regulations

Information

Type

Reference Document

Regulated products

Medical Devices

Published

November 2, 2021

Last updated

February 24, 2023

Description

Reference document FAQ MD regulation - Notified bodies in your application process

Organization

National Agency for the Safety of Medicines and Health Products (ANSM) 🇫🇷

Country / Region

France

License

Other (Non-Commercial)

Feedback

Suggest an improvement to this page

1 Main file

FAQ règlement DM – Organismes notifiés

Updated on February 24, 2023

html

URL: https://ansm.sante.fr/documents/reference/faq-reglement-dm-organismes-notifies
Permalink: https://data.openrid.co/en/datasets/r/6d2e51c8-1e1b-405e-b67f-dfd0c391a124
MIME Type: text/html

Created on: November 2, 2021
Modified on: February 24, 2023