Regulatory Affairs, Medical Devices

Navigate the latest ISO & MDR updates and accelerate Biocompatibility compliance

IVD School: understand the fundamentals of in vitro diagnostic regulatory affairs and accelerate time to market

Navigate The Medical Device Regulatory Landscape In Latin America For Faster Approvals

Capitalise on the opportunities of medical device software under the EU MDR and accelerate your market success

Consolidate your strategies for labelling and UDI compliance under the EU MDR and IVDR

Apply Post Market Surveillance, Risk Management and Vigilance requirements under the EU MDR and IVDR with confidence