Dietary Supplements

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In general, the Part 111 GMP requirements, although similar, are less stringent and tend to be more flexible than the Part 211 GMP requirements.

Mar 4, 2015

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

CHPA applauds FDA's efforts to amend labeling regulations for conventional foods and dietary supplements in order to provide updated nutrition information to consumers.

Aug 1, 2014

Comments regarding guidance for clinical investigators, sponsors, and institutional review boards on investigational new drug applications - Determining whether human research studies can be conducted without an investigational new drug application.

Apr 7, 2014

There are several scientific and technical issues the agency should consider prior to issuing a final determination regarding partially hydrogenated oils (PHOs).

Mar 7, 2014

CRN and CHPA take this opportunity to share our views on the Food and Drug Administration’s Federal Register notice entitled, “Tentative Determination Regarding Partially Hydrogenated Oils; Request for Comments and for Scientific Data and Information.”

Mar 7, 2014

Echoing earlier comments submitted to the agency, CHPA and its member companies marketing dietary supplement products support the presumption of safety for dietary ingredients outlined in the 1994 passage of DSHEA.

Oct 24, 2013

We take this opportunity to voice our support of comments submitted by the Council for Responsible Nutrition (CRN) regarding the appropriate interpretation of the term “chemically altered” under Section 413(a)(1) of the Federal Food, Drug, and Cosmetic Act.

Jul 12, 2013

We take this opportunity to voice our support of comments submitted by the American Herbal Products Association regarding proposed revisions to the agency's Draft Guidance on New Dietary Ingredient Notification.

May 10, 2013

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