Creating an Effective Validation Master Plan
The Food and Drug Administration (FDA) is tasked with protecting the public health by ensuring the safety, efficacy, and security of the nation’s food supply, human and veterinary drugs, biological products, medical devices, vaccines, and other products. In order to fulfill its mission, the FDA requires that all products under its domain meet guidelines outlined in current Good Manufacturing Practice (GMP) regulations. These guidelines serve to ensure that end products are free from contamination and consistent in manufacture, that the manufacturing process has been well documented, that personnel are well trained, and that the product has been checked for quality throughout the manufacturing process.
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