the voice of the natural health consumer

Supplements

Antioxidant Misinformation

Minneapolis, MN, May 7, 2008 - As natural health consumers, we all know that our vitamins, supplements and nutrients are frequently and consistently targeted by the malicious or misinformed who question their safety or legitimacy. Citizens for Health Senior Policy Advisor, James Gormley, shares his perspective on some of the more recent propaganda.


TAKE ACTION: Citizens for Health Joins AHPA in Opposing Irradiation of Supplements

For Immediate Release

Contact: Jim Turner, 202.462.8800

Washington, D.C., December 17, 2007 - Citizens for Health has joined with the American Herbal Products Association in opposing a petition filed with the Food and Drug Administration (FDA) to allow the use of ionizing radiation for the control of microbial contamination on dietary supplements and dietary ingredients.


FDA Accepting Comments on Adverse Event Reporting

Washington, D.C., October 15, 2007 - Today the FDA released  and is accepting comments on its guidance on requirements for the reporting of serious adverse events under the Dietary Supplement and Nonprescription Drug Consumer Protection Act. 


FDA's "Alternative" Reality

Citizens for Health Senior Policy Advisor, James Gormley, reports on the FDA's "Guidance for Industry on Complementary and Alternative Medicine Products and Their Regulation by the Food and Drug Administration"


Take Action Now: Health Freedom Protection Act Reintroduced

Take Action: Support H.R. 2117Take Action: Support H.R. 2117

 

 

Washington, May2, 2007 - Congressman Ron Paul (R-TX) has reintroduced the Health Freedom Protection Act, H.R. 2117, which will end FDA and FTC censorship of food-based health claims and ensure that consumers are given truthful and full information about the science supporting the health-enhancing effects of foods and dietary supplements.


What Happens in New York, Doesn't Stay in New York

Citizens for Health Board member, James Gormley, warns us about proposed laws in New York that could affect your access to supplements.


The Return of L-Tryptophan

By James J. Gormley

“The story of L-tryptophan,” said Marc Ullman, partner at New York City-based Ullman, Shapiro and Ullman, “is a story of the disappearance (and re-appearance) of a beneficial, well-liked ingredient from the marketplace due to a combination of regulatory concerns and marketplace overreaction.”


Dietary Supplement GMPs Finally Released

From The Natural Products Industry Insider - The Food and Drug Administration (FDA) released a final rule on current Good Manufacturing Practices (cGMPs) for dietary supplements.


Citizens for Health Files Its Comments on CAM Guidance - Send Yours Today!

    Official Comment Period Ends,      Pressure on the FDA Heats Up 

WASHINGTON, June 1st, 2007 - Citizens for Health (CFH) has filed its comments on the FDA's "Guidance for Industry on Complementary and Alternative Medicine Products and Their Regulation by the Food and Drug Administration", a document stating the agency's interpretation of existing policy governing supplements, alternative practioners, and non-traditional modalities.


FDA Calls Citizens for Health, Announces Re-opening Comment Period on CAM Guidance

On May 23rd, the FDA point person on the CAM Guidance called Executive Director, Frank Herd, Jr, to announce that the comment period was re-opened.


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