Veristat Resource Library

Impact of New Medical Device EU Regulation (MDR) on the Development of Drug-Device Combination Products

In this webinar presentation, Veristat Regulatory experts will present the changes between the Medical Devices Directive and the Medical Devices Regulation and highlight the differences between the requirements and procedures for different types of Drug-Device Combination Products under the MDR. The webinar will include a Q&A session with our experts.