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Press Release New medtech regulations

Industry supports European Commission in strengthening medical devices legislation

Posted on 09.02.2012


Brussels, 9 February 2012 – The European medical technology industry recognises the need to improve the effectiveness of the current European regulatory framework for medical devices. Eucomed, the European industry association for medical technology, appreciates the European Commission’s swift reaction and clear proposal for a joint plan of immediate measures to strengthen the European medical devices legislation. After analysing the Commission’s proposal, Eucomed believes the measures are balanced and appropriate and will have a positive effect on patient safety.

Eucomed has called for a legal framework that provides a consistent, EU-wide regulatory approach through improved coordination, evaluation and certification of medical devices; consistent and comprehensive implementation across all EU Member States, as well as efficient vigilance and market surveillance systems. Europe needs smart regulation that makes efficient and effective use of existing resources and involved structures (European Commission, Competent Authorities, Notified Bodies and industry) so as to retain a simple, adaptable and highly efficient system and merit public confidence.

The European medical devices legislation is currently under revision and Eucomed has suggested six steps to a smarter legal framework for medical devices:

  1. Only the best Notified Bodies;
  2. One approach to vigilance and market surveillance;
  3. Strengthened harmonised standards;
  4. Consistent implementation of guidelines;
  5. Increased transparency;
  6. An integrated approach: better coordination and management.

For more information download the following documents: