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Bringing EU Commission, Competent Authority, Notified Body and industry experts together to discuss the evolving global regulatory landscape
9 focused tracks: EU MDR. IVD Regulation and Strategy. Software and AI. Law and Compliance. Post Market Surveillance & Vigilance. Clinical Evaluations & Investigations. Global Market Regulations. Biocompatibility. Drug Device Combination and Borderline Products.
This announcement is a third-party event and is not organised by BIOPRO Baden-Württemberg GmbH itself. BIOPRO provides this announcement for distribution and information purposes and, despite careful examination of the content reproduced, assumes no liability for the correctness or subsequent changes by the organizers. If you have any questions, please contact the organizer directly.
