Clin-r+ Ltd can assist medical device manufacturers with gap assessments and the transition to MDR. An EU MDR Readiness checklist can assist in efficient planning. It should be a practical tool that ensures you are compliant with the regulations.
A Medical Device Regulation transition period extension request was submitted at the EPSCO Council on 9 December 2022, and a proposal was available by 6 January 2023. CLIN-r+ highlights the key elements of that proposal and the EU MDR deadlines.
We provide services globally, so reach out via this contact page and we will reach out to you, within 12 hours to discuss how we can help.
