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| FDA Guidance Manual on Supplement Facility Inspections, Sampling, and Imports: How Compliant Are You? (Mar 2021) |
According to the U.S. Food and Drug Administration (FDA), its Compliance Programs exist to provide instructions to FDA personnel for conducting activities to evaluate industry compliance with the Federal Food, Drug, and Cosmetic Act and other laws administered by FDA. On September 30, 2020, FDA released its Compliance Program Guidance Manual (CPGM) titled “Dietary Supplements – Foreign and Domestic Inspections, Sampling, and Imports.” Per FDA, the goal of this CPGM is to ensure companies consistently manufacture dietary supplements of acceptable quality and minimize consumers’ exposure to adulterated and/or misbranded dietary supplements.
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Item
Number: WEB007
Shipping Weight: 0lbs. 0oz. |
| Price:
$199.00 |
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| AHPA webinars bring together subject matter experts to cover a wide range of diverse topics relevant to the herbal product and dietary supplement industries – including regulatory compliance, technical issues, and current events. AHPA’s industry-leading educational programming is designed to meet the evolving needs of members and the industry. |
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