Regulatory affairs specialist
HaryanaNeuvoo
...Proficient in updating the documents in accordance with the European Union Medical 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 [...]
Category Education, Training, & Library
19 days ago in Labor24