Transition continues for medical devices and IVDs from the current European directives to new European regulations. The Active Implantable Medical Device Directive (AIMDD) and Medical Devices Directive (MDD) will be transformed into the new Medical Device Regulation (MDR). For IVDs, the In Vitro Diagnostic Directive (IVDD) will be replaced by the In Vitro Diagnostic Regulation (IVDR). This workshop will divide into two tracks. Each track will reconfirm the essentials of the current directives, address the changes introduced by the regulations and provide input for planning a successful transition process. Experts will provide attendees with a solid understanding of what remains the same, what changes and the new requirements that must be addressed.