Latest news
New medtech regulations
New adverse event terminology to be implemented in Europe
Posted on 01.12.2017
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New medtech regulations
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New list of harmonized standards for medical devices
Posted on 01.12.2017
New medtech regulations
CAMD publishes IVDR and MDR Implementation Roadmap
Posted on 01.12.2017
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New medtech regulations
IVDR/MDR implementation – notified body publications
Posted on 01.12.2017
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Newsletter
MedTech Europe signs the Joint Reaction Paper “For an Ambitious EU Industrial Strategy: Going Further”
Posted on 25.10.2017
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Interactions with the Medical Community
HCO/PCO Webinar – How to apply the MedTech Europe Code in France
Posted on 28.09.2017
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New medtech regulations
Stakeholder Consultation on the EU blood and tissues and cells legislation
Posted on 28.09.2017
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Responsible Business and Supply Chain
MedTech Europe on CEN/CENELEC Seminar on Standardisation (21 September 2017)
Posted on 28.09.2017
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