ePMCF
CIMS eletronical Post Marked Clinical Follow-up ePMCF is build upon the backbone of CIMS eSystems functionality. CIMS ePMCF contains the elements of post market clinical follow-up minimum requirements from the 2017/745 MDR regulation. All documents can be created on templates, uploaded from other systems, edited and follow the path of review, approval, eSignature, storage as all CIMS eSystems.
Activities under the PMCF can also be created and stored related to the MDR requirements.