Medical device regulatory expert
HaryanaNeuvoo
...(Sot A); evaluating the data from MAUDE, HPRA or MHRA c ompiling information from various sources Update and review Periodic Safety Update Reports (PSUR) for medical devices. Prepare/ update Clinical Evaluation Reports (CER) in compliance with regulatory requirements for Medical Device Technical File (MDTF) [...]
Category Education, Training, & Library
3 days ago in Labor24