Presentation is loading. Please wait.

Presentation is loading. Please wait.

The European Association Medical devices

Similar presentations


Presentation on theme: "The European Association Medical devices"— Presentation transcript:

1 The European Association Medical devices
Notified Bodies Presentation 2019

2 Context of TEAM-NB DG GROW TEAM-NB representatives CEN CENELEC EMA
NBRG NB-MED MDEG NBOG COEN Experts Groups EUDAMED, IVD, CIE Vigilance logo I M D R F A Switzerland Canada Australia New Zealand USA Japan, … CPME AMDR, EAAR, COCIR, EUROMContact, MedTech Europe, FIDES, EDMA, EUROM UEAPME, CMC Health Professionals Notified Bodies Manufacturers 28 Competent Authorities National Accreditation Bodies Authorised Representatives Accreditation Notification 2 2019 Presentation

3 TEAM-NB Communication with Promote technical and ethical standards
Aims: Communication with European Commission Competent Authorities Industry Promote technical and ethical standards Participate in improving the legal framework Contribute to harmonization Represent Notified Bodies 3 2019 Presentation

4 TEAM-NB 2019 Presentation

5 Code of Conduct V 3.4 Mandatory to sign for TEAM-NB members
Version 3.4 approved Available on website 2019 Presentation

6 Interpretation of the new regulations
Team-NB established working groups already from April 2016 Aim: formulate an analyse of the new regulations and propose to the members Procedures to be put in place To-do lists to be done to submit application for designation and/or wait for implementing acts Help members to be designated Allow harmonisation Classification & Conformity Assessment NB requirements Clinical Vigilance 6 2019 Presentation

7 Team-NB: MDR Designation process
Data collected in December 2018 with responses of 22 out of 24 members (knowing that 57 Notified Bodies currently designated for MDD and AIMD) 7 2019 Presentation

8 Team-NB: IVDR Designation process
Data collected in January 2019 with responses of 20 out of 24 members (knowing that 22 Notified Bodies currently designated for IVDD with 10 members)  1 more member intend to apply for IVDR 8 2019 Presentation

9 Designation of notified bodies
Notified body designated according to MDR / IVDR before certification of manufacturers Steps List of codes published in an implementing act - November 2017 Introduction of an application for designation by NBs On November 26th, 2017 at the earliest 80% of the members did it 2017 9 2019 Presentation

10 Designation of notified bodies
Steps (… to be followed) Joint audit assessment April 2018: 3 assessments performed ... Conformity assessment bodies designated on NANDO Transparency of the designation process (on-going survey) All codes to be covered 10 2019 Presentation

11 MDR: From May 26th 2020 to May 26th 2024
Transition period MDR: From May 26th 2020 to May 26th 2024 11 2019 Presentation

12 IVDR: From May 26th 2022 to May 26th 2024
Transition period IVDR: From May 26th 2022 to May 26th 2024 12 2019 Presentation

13 CE mark after "Entry into Application"
Transition period CE mark after "Entry into Application" Compliance with MDD or AIMD No significant change in design and intended purpose Application of the requirements of the Regulations related to Post-market surveillance, Market surveillance, Vigilance, Registration of economic operators and devices, NB remains in charge of surveillance Contract between Manufacturers and NBs update to be signed to allow surveillance audits 13 2019 Presentation

14 Regulation tools Commission tools Under the MDCG supervision
Common specifications New instrument to be adopted by implementing acts which manufacturers will need to apply Delegated and implementing acts instrument to precise regulation articles 14 2019 Presentation

15 European databank on MD (EUDAMED)
Use of a medical device nomenclature mandatory Data to be uploaded to collate and process information regarding MD SRN – single registration number UDI – unique device identifier -> traceability aspects of conformity assessment notified bodies certificates clinical investigations vigilance and market surveillance 15 2019 Presentation

16 Contacts www.team-nb.org Management:
Management: Guy Buijzen – president Kevin Butcher – vice president Corinne Delorme – secretary Hans Heiner Junker – vice president Alexey Shiryaev - treasurer Françoise Schlemmer -Director and Secretariat 16 2019 Presentation

17 Members


Download ppt "The European Association Medical devices"

Similar presentations


Ads by Google