Food and Drug Administration DEFINITION: The FDA is responsible for protecting the public health by assuring the safety, efficacy, and security of human and veterinary drugs, biological products, medical devices, our nation's food supply, cosmetics, and products that emit radiation.
This paper explores how medical device can seamlesslyembed methodologies such as hazard analysis, fault tree analysis (FTA)and failure mode effects analysis (FMEA) into their developmentprocesses—helping them develop safe, FDA-compliant products.
This white paper presents a guideline to help you select an ERP system for your FDA validation. Explore a five phase software acquisition life cycle model to help you accomplish these objectives as efficiently as possible.
This whitepaper addresses the trends surrounding Supply Chain Risk Management (SCRM) and the strategies that manufacturers are using to mitigate risk from their supply network. It contains a case study about how one manufacturer is viewing real-tim...
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