Regulatory affairs lead
HaryanaNeuvoo
...medical devices. Prepare/ update Clinical Evaluation Reports (CER) in compliance with regulatory requirements for Medical Device Technical File (MDTF) Perform gap assessment of the available version of CER with respect to MEDDEV Rev. 4 and MDR Experienced in IVD regulatory Affairs, EU MDR/IVDR Gap Analysis, Performance [...]
Category Education, Training, & Library
7 days ago in Labor24