Regulatory Affairs, Quality & Risk Management
Advance your expertise in EU certification and international regulatory strategies. Gain in-depth knowledge of MDR/IVDR, MDCG guidances, ISO 13485, ISO 14971 and other technical standards, as well as labelling requirements, UDI and EUDAMED.
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We are happy to provide you with personal and individual advice.
Our professional development portfolio is extensive. We would be pleased to discuss your requirements with you personally and help identify the most suitable options from our range of offerings. Let our professional development experts advise you and feel free to contact us today.
Verena Planitz
Conference Manager Healthcare
+49 6221 500-655
v.planitz@forum-institut.de