Orientations réglementaires
Annex I: Template CAPA plan and assessment thereon
Publié 1 oct. 2024
Référence
MDCG 2024-12 Annex I Form
Source
MDCG
Thème
Notified bodies
Publié
1 oct. 2024
Langues
EN
© European Union — European Commission, DG SANTE. Reuse under CC BY 4.0.
Questions and answers: Requirements relating to notified bodies
Publié 1 févr. 2025
Application form to be submitted by a conformity assessment body when applying for designation as notified body under the medical devices regulation (MDR)
Publié 1 janv. 2025
Annex to Application Form & PAR Template MDR (List of documents)
Publié 1 janv. 2025
Application form to be submitted by a conformity assessment body when applying for designation as notified body under the in vitro diagnostic devices regulation (IVDR)
Publié 1 janv. 2025