Medical Device Manufacturers Can Leverage ERP/CRM Software to Facilitate FDA Compliance
The US Food and Drug Administration (FDA) requires pharmaceuticals and medical device companies to comply with numerous standards. Medical device manufacturers

disbursement software  module for easy email disbursement. Electronic Signatures A fairly new requirement of FDA-regulated medical device manufacturing companies concerns Section 21 Part 11 of the Code of Federal Regulations. The code establishes the standards by which the Food and Drug Administration will accept electronic records and electronic signatures as equivalent to paper records and handwritten signatures. The rule governs electronic records throughout their lifecycle from creation through modification, storage, and fi

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