• (0)
    Full text of EU MDR (Medical Device Regulation)
    EU MDR Chapter 8 Article 101

    Article 101 – Competent authorities

    The Member States shall designate the competent authority or authorities responsible for the implementation of this Regulation. They shall entrust their authorities with the powers, resources, equipment and knowledge necessary for the proper performance of their tasks pursuant to this Regulation. The Member States shall communicate the names and contact details of the competent authorities to the Commission which shall publish a list of competent authorities.

    IMPLEMENT ISO 13485 & MDR
    BY YOURSELF

    SEE HOW IT WORKS

    • Optimized for small and medium-sized companies
    • Costs up to 80% less than using consultants
    • Expert consultations and unlimited email support available
    • Created by Advisera, the leading website for compliance