The EU's Competent Authorities for Medical Devices, or CAMD, was created to improve cooperation and communication on the risk assessment and monitoring of medical devices. CAMD is an umbrella group under which national authorities work together toward improvement on common tasks. 

Organiser: Federal Ministry of Health

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Bundesinstitut für Arzneimittel und Medizinprodukte

Fachgebiet Internationaler Austausch und Konferenzen

+49 228 99307 3183