The CAMD network is delighted to be able to publish the high-level Medical Devices Regulation/In-vitro Diagnostics Regulation (MDR/IVDR) Roadmap.
This is the result of a number of months collaborative work by the network and the European Commission as well as benefitting from considerable stakeholder input. The working groups challenged with delivering the targeted outputs are now working up detailed work plans. The detail in this document is likely to evolve as the work programmes develop. Answers on high frequency or critical issues will be developed as an aid to consistent implementation across all geographies.
Download the Medical Devices Regulation/In-vitro Diagnostics Regulation (MDR/IVDR) Roadmap from the CAMD Implementation Taskforce.