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Keywords: Regulatory Affairs Executive with a medical device company in Bangalore,
Location: Bangalore, Karnataka
Page: 1
Regulatory Affairs Executive with a medical device company in Bangalore
design dossier as per CE (EU MDR), ISO 13485 and USFDA guidelines. Experience in preparation of Device master file... 14971. Knowledge on post market surveillance, PMCF, clinical evaluation and UDI. Exposure to EU MedicalDevice Regulation...