NVFG ClinOps Medical Device meeting |
ACS CEO presented on AE reporting under the MDR.
EU Commission issues decision flowchart for devices covered by the MDR transitional period |
EU Commission issues guidance on the summary of the clinical study report |
CEO presentation on Adverse Events handling under the MDR (2017/745) |
EU Commission adopts decision for safe EU-US data flows |
MDCG updates guidance on significant changes for MDD and AIMDD devices |