Medical devices

MD4/IVD4: UK MDR – Current requirements and future perspectives for medical devices and in vitro diagnostics

By 2024-11-08T06:56:00

MD4 - AshleighBatchen

Key points:

  • UK Conformity Assessed (UKCA) marking remains a requirement for placing medical devices on the UK market
  • The recognition of European conformity (CE) marked medical devices has been extended to 2030

To read more key points and the session summary, log in as a member or register for free using the links below.

How to read this journal article 

Thank you for visiting Regulatory Rapporteur. Journal articles are restricted to registered users and TOPRA members.

Already a member or have an account? Sign in.

1. REGISTER FOR FREE

Free access to selected content

Register now to continue to access industry news, editorials and podcasts plus one member-only journal article each month.

  • Create your own library to save your favourite content.
Create a free account

2. Members login

Already a TOPRA member?

Log-in now using your MyTOPRA credentials, for unlimited access to all Regulatory Rapporteur journal articles, the online archive and latest industry news and podcasts.

Login

3. JOIN TOPRA

TOPRA membership

Become a TOPRA member and join our global regulatory affairs community.

  • Great savings on our events and training.
  • Be part of our dynamic international community.
  • Contribute to the profession.
  • Grow your skills and knowledge.
  • Take your career to the next level.

Become a member