*For TFHC Partners only | In 2020 new European Medical Device Regulation (MDR) will be enforced. MDR imposes numerous changes for manufacturers, importers and distributors of medical devices, biotech and pharmaceuticals such as new requirements for classification of medical devices, stricter safety requirements and post-market surveillance. Want to know how MDR impacts you? And want to learn how to prepare your business for upcoming changes? Join the TFHC-Emergo seminar: Getting Ready for EU MDR to become familiar with the basic changes post-MDR implementation and receive advice from our experts to prepare yourself for MDR.
What to expect?
Our speaker Annette van Raamsdonk, LL.M., joined the Emergo team in The Netherlands in 2017 and is bringing an extensive regulatory affairs background with her. She gained significant experience with a wide variety of medical devices while working at TÜV Rheinland as well as during her time serving as an Inspector of Medical Technology at the Dutch Health Care Inspectorate (IGZ/IGJ). Annette represented the IGJ within the European Competent Authorities’ working group for Compliance and enforcement and is currently the lead contact person at Emergo for European Competent Authorities.