Pages Messages Home CAMD Aims and Objectives CAMD Executive Group MDR/IVDR Implementation MDR/IVDR Implementation Taskforce MDR/IVDR Transition Subgroup Joint Action Projects JAMS 2.0 JAMS 2.0 Work Packages – Overview JAMS 2.0 Participants 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 Forum Account Settings User Login Logout Register Password Reset Sitemap Terms & Conditions Cookie Policy Privacy Policy Posts by category Category: Events Coordination and governance of the regulatory system for medical devices at the EU level: publication of a consensus statement from the EU Competent Authorities to the EU Commission 55th CAMD meeting statement Medical Devices and In Vitro Diagnostics Regulations: publication of a consensus statement from the EU Competent Authorities to the EU Commission 54th CAMD meeting statement 53rd CAMD meeting statement 52nd CAMD meeting statement CAMD Statement – 50th CAMD Plenary meeting MDR, 2021 may 26th, Date of Application is now ! 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 Questions and Answers on Certificates of Free Sale and Article 60 of Regulation (EU) 2017/745 on medical devices (MDR) The JAMS layman’s report is now available online! 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 Update from HMA Core Group: Letter from the HMA Core Group of Medical Devices to the European Commission 51th CAMD meeting Statement 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 Categories CAMD Meetings Mondays for future
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