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The Food and Drug Administration (FDA) started enforcing Good Manufacturing Practice requirements for all Dietary Supplement manufacturers in 2010. Since then, they have published the results of their inspections and the warning letters they issue when manufacturers fail to come into compliance.  The experts at InstantGMP™ understand that current Good Manufacturing Practices (cGMP) for dietary supplements  can be complex and confusing.  They prepared this series of articles and videos that describe the requirements for manufacturing these products in compliance with the FDA’s requirements. This page provides links to the InstantGMP™ Compliance Series articles. Different parts of the series focus on the different aspects of Good Manufacturing Practices.

Check out our solution for Dietary Supplement manufacturers, InstantGMP™ MES and be sure to watch the online demonstration. To learn more about the tenants of Good Manufacturing Practices, be sure to read about required documentation, including: Master Batch Records and Batch Production Records, as well as learning about the differences between the two types of production records. Want to get on the path to GMP compliance? Standard Operating Procedures are a great first step to set up the quality process for dietary supplement manufacturers.

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