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FDA 21 CFR Part 210

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FDA 21 CFR Part 210

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FDA regulation 21 CFR Part 210

The Food and Drug Administration’s (FDA) standards for Title 21 of the Code of Federal Regulations (CFR), also known as the FDA 21 CFR, provide a clear and concise set of regulations.

A specific focus of FDA 21 CFR Part 210 is current Good Manufacturing Practices in the processing of manufacturing, packaging or holding of drugs.

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