Why a regulatory information strategy is critical for successful MDR/IVDR transitions

The significant changes introduced with the MDR and IVDR regulations have created both a need and an opportunity for RA teams to leverage a better approach to regulatory information management. This webinar explores the new information requirements associated with MDR/IVDR including GSPRs, UDI/EUDAMED, and Post-market surveillance and reporting, and and how a shift to a product-centric vs project-centric approach can make information more accessible and usable across teams and processes.