Pages Messages Home CAMD Aims and Objectives CAMD Executive Group MDR/IVDR Implementation MDR/IVDR Implementation Taskforce MDR/IVDR Transition Subgroup Joint Action Projects Market surveillance of medical devices (JAMS) Overview of work packages Participants Instructions for use of medical devices (COENJA2014) Overview of work packages Participants Resources Glossary News Locations Contact Forum Account Settings User Login Logout Register Password Reset Sitemap Terms & Conditions Cookie Policy Privacy Policy Posts by category Category: Events JAMS Stakeholder Conference Held In Brussels On Dec. 12th 2019 JAMS featured in the EU Health Programme High Level Conference 42nd Meeting of the Competent Authorities for Medical Devices network 41st Meeting of the Competent Authorities for Medical Devices Category: Health EUDAMED State of play : Open letter from the CAMD Executive Group Patient safety – the focus for all Competent Authorities for Medical Devices (CAMD) members Category: Other Joint Action on Market Surveillance of Medical Devices (JAMS) releases progress update Category: Regulatory JAMS publishes stakeholder leaflets Available now: MDR and IVDR transitional FAQs Medical Devices Regulation/In-vitro Diagnostics Regulation (MDR/IVDR) Roadmap Category: Wellbeing General Short Talk Categories CAMD Meetings CEG News
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