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Expert perspectives focused on the latest bioanalytical topic & trends

The Importance Of GMP Certification In Drug Development

Production and sale of therapeutic drugs requires tight control over the manufacturing, processing, and labeling of these products to ensure the safety of the end user. In the United States, regulations for maintaining the quality of medications such as these are under the jurisdiction of the Food and Drug Administration (FDA). They are referred to as Good Manufacturing Practice (GMP) or Current Good Manufacturing Practice (CGMP) regulations. GMP regulations mandate

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