Medical device regulatory expert
HaryanaNeuvoo
...Device Directive (EU MDD 93/42/EEC), the European Medical Device Regulation (EU MDR XXXX/XXX, MEDDEV 2.7/1 Guidelines for the Evaluation of Clinical Data Responsible to provide medical inputs with relevant and updated clinical evidence and to monitor the execution of other strategic documents as PBRERs, ACOs, DSURs, Clinical [...]
Category Education, Training, & Library
3 days ago in Labor24