anteris medical and Bellingswood periodically organize network meetings and workshops on various topics related to the regulatory requirements of medical devices. The aim of these events is to promote a platform for the exchange of experiences among experts, and to inform about the latest developments in Regulatory Affairs.
Our first event covering MDR/IVDR and Clinical Evaluation in Munich was completely sold out. Experts from the biotech, pharmaceutical, and medical device industries, such as developers and manufacturers, CROs, market researchers, and consultants, came together to discuss the latest developments and challenges of new regulations concerning medical devices, drug/device combination products, and IVD devices.
More informations concerning upcoming events will be soon our homepage.