Good Manufacturing Practices

Press Releases and Statements

CHPA Statement on Justice Department and Federal Partners Announcement of Enforcement Actions Against Illegal Products Sold as Supplements

Nov 17, 2015

Articles

New York Attorney General Questions Certain Herbal Dietary Supplements – But Scientists, Experts Say the AG Used the Wrong Test

Scientific experts familiar with herbal products and their testing methods maintain that the DNA barcode test is not an appropriate method to determine what is in an herbal dietary supplement.

Feb 23, 2015

DSHEA

blue and orange stacked shipping containers

Submission

AESGP and CHPA Response to the EU-US Call for Industry Input on Regulatory Issues for Possible Future EU-US Trade Agreement

Sep 28, 2012

OTC Medicines

red capsules being sorted in a circular hopper

Submission

Comments to FDA: Program Priorities in the CFSAN

CHPA requests CFSAN to commit to the finalization of Good Manufacturing Practices for dietary supplements as one of its highest priorities for FY 2005.

Aug 9, 2004

woman worker in protective clothing operating production of tablets in sterile environment

Submission

Comments to FDA: cGMPs for Dietary Ingredients and Dietary Supplements

CHPA supports rules governing the regulation of dietary supplements as a special type of food. The association has long advocated Good Manufacturing Practices for dietary supplements.

Aug 8, 2003

New Dietary Ingredients

Quality

FAQs

FAQs About Homeopathic Medicine

Learn about the uses, safety, and regulation of homeopathic medicines in the U.S.

OTC Medicines

Ingredient Safety

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Fact Sheet: Dietary Supplements as Regulated Products

CHPA supports the regulatory authorities governing dietary supplement manufacturing, labeling, and marketing and works to ensure the availability of safe dietary supplements.

New Dietary Ingredients

hands in sterile gloves holding manufactured white tablets

Industry Self-Regulation for Dietary Supplements

Dietary Supplement Component Supplier Qualification

This document serves as a voluntary guideline to assist manufacturers of dietary supplements with compliance with the dietary supplement current good manufacturing practice (cGMP) requirements of the US FDA 21 CFR §111.