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ACTION ALERTS
Home
Advocacy Info
Resource Center
State Organizations
About
NHFC

Federal Regulation Information

FDA Homeopathic Products:
NHFA to FDA, March 2018, Formal Comments in response to the FDA proposed Draft Guidance entitled: Drug Products Labeled as Homeopathic: Guidance for FDA Staff and Industry, Docket ID. FDA-2017-D-6580, Food and Drug Administration – Center for Drug Evaluation and Research (CDER) in cooperation with the Center for Biologics Evaluation and Research (CBER), December 2017.

CDC Communicable Disease:
NHFA to CDC, September, 2016, Formal Request for the Withdrawal of the CDC’s Notice of Proposed Rulemaking entitled: Control of Communicable Disease, Docket No. CDC-2016-0068, Department of Health and Human Services, Center for Disease Control and Prevention, August 2016.

FDA New Dietary Ingredients:
NHFA November 2011, Formal Comments in response to the FDA proposed Draft Guidance: “Draft Guidance for Industry; Dietary Supplements: New Dietary Ingredient Notifications and Related Issues; Availability”, Docket No. FDA–2011–D–0376 20, July 2011.

Creating New Laws:
Miller, D, 2009. Creating New Health Care Laws and Regulations, Alternative and Complementary Therapies.

Dietary Supplement Product Labeling:
Miller, D, 2007. Freedom of Speech and Truthful Information in Health Care, Alternative and Complementary Therapies.

CAM and the FDA:
NHFA to FDA, 2007, Formal Comments in response to the FDA proposed Draft Guidance entitled: “Guidance for Industry on Complementary and Alternative Medicine Products and Their Regulation by the Food and Drug Administration” Docket ID. 2006d-0480, Department of Health and Human Services, Food and Drug Administration, December 2006

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info.nhfa@nationalhealthfreedom.org
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St. Paul, MN 55116-1863
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