AHPA Guidance

AHPA guidance documents

AHPA produces these guidance documents on specific topics to help the industry comply with applicable laws and regulations and institute best practices that help ensure quality and transparency.

Additional guidance is available in AHPA's Guidance Policies >>

Guidance for Addressing FDA cGMP Inspections of Dietary Supplement Facilities

Understand your rights and obligations when FDA conducts a cGMP inspection

This Guidance for Addressing FDA Inspections of Dietary Supplement Facilities has been prepared to assist AHPA members in understanding their rights and obligations when the U.S. Food and Drug Administration conducts an inspection of a facility in which dietary supplements or ingredients are manufactured, processed, packed or held. It provides descriptions and analyses of the current federal laws that are relevant to inspection of dietary supplement facilities and suggestions of how to prepare for and conduct inspections in a manner that fully complies with these laws.

White Paper: Standardization

Standardization of Botanical Products

This paper describes the many factors that contribute to the proper standardization of a botanical product

Manual for Alcohol Tax Drawbacks for Manufacturers of Nonbeverage Products Sold as Liquid Herbal Supplements

Guidance to help manufacturers understand and conform to Federal Regulations that govern the drawback of prepaid excise tax on alcohol used in the products of nonbeverage products

AHPA's Guidance Documents for the Manufacture and Sale of Botanical Extracts

AHPA's Guidance Documents for the Manufacture and Sale of Botanical Extracts (2001)

AHPA's Guidance Documents for the Manufacture and Sale of Botanical Extracts
RSS
123

2018 Annual Fund Sponsors

           

AHPA appreciates the support of its sponsors, but does not endorse, recommend, or provide a warranty for any sponsor company, its products or services. AHPA has no responsibility for any transaction entered into with any of these companies.