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CGMP stands for current good manufacturing practice. It is a set of regulations enforced by the US Food and Drug Administration to ensure the quality and safety of pharmaceutical products.
Pharmaceutical companies and manufacturers who produce drugs are required to comply with CGMP regulations.
CGMP forms are typically filled out online through the FDA's electronic submission system.
The purpose of CGMP is to establish minimum requirements for the manufacturing, processing, packaging, and holding of pharmaceutical products to ensure their safety and quality.
CGMP reports must include information on the manufacturing processes, quality control procedures, and any deviations or non-conformances.
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