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How Do Integrated Audits Work? A Comprehensive Guide
In today’s fast-paced industry, companies require multiple certifications to meet regulatory, safety, and market access requirements. A food manufacturer, for instance, would typically need…
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Detailed Cosmetic FDA Regulations in the U.S
Cosmetic FDA regulations changed dramatically when the U.S. Congress passed the Modernization of Cosmetics Regulation Act (MoCRA), giving FDA new powers over the cosmetics…
Detailed Supplement Label Claims Guide in the U.S
What Can You Say on a Dietary Supplement? For a supplement product, one critical question that needs to be answered before the label is…
What is ISO 22716 and Is it Mandatory for Cosmetics Manufacturers?
For cosmetic manufacturers, the ISO 22716 guideline is the most important standard to comply with. ISO 22716 is the international guideline for Good Manufacturing…
What is Required for 21 CFR Part 111 Compliance?
21 CFR Part 111 is the FDA’s current good manufacturing practice rule for dietary supplements. It applies to companies that manufacture, package, label, or…
GMP Audit Checklist – CGA Resource Guide
The CGA GMP audit checklist is a structured tool that is used to assess whether the facilities of a manufacturer complies with Good Manufacturing…
Detailed Non-GMO Certification Requirements
Non-GMO certification requirements often vary as not all ingredients carry the same GMO risk. Corn, soy, canola, sugar beet, and some derivatives usually require…
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