Industry News & Our Position
Standard Process' Position on "Dietary Supplment and Non-Prescription Consumer Protection Act"
(12/16/06) - Standard Process believes it is appropriate and responsible for nutritional supplement companies to report Serious Adverse Events (SAEs).

The "Dietary Supplement and Non-Prescription Consumer Protection Act," as it passed both the Senate and the House of Representatives, will require reporting SAEs for nutritional supplements and OTC medicines. The legislation reflects industry input, protects manufacturers from burdensome FDA regulation, and brings a level of credibility and transparency to the fact that SAEs resulting from supplement use are rare.

We, joined with American Herbal Products Association (AHPA), United Natural Products Alliance (UNPA), and other dietary supplement trade associations, support the legislation.

For more information about the "Dietary Supplement and Non-Prescription Consumer Protection Act," visit:

Position Statements
Drug Safety Issues Lead Consumers to Consider Natural Alternatives - 03/05
New Echinacea Study Not Relevant to Informed Practice - 01/06
Position on Dietary Supplment and Non-Prescription Consumer Protection Act - 12/06
Position on FDA's Proposed Guidance for Industry on Complementary and Alternative Medicine Products
Standard Process' Position Regarding the Codex Alimentarius Commission
Standard Process Inc.
Post-Purification Diamond
New Post-Purification Program

What comes next after purification? Post-purification! Help your patients continue to manage their weight and stay healthy.

Resale Policy | Promotional Rules | FAQs | Trademarks | Terms of Use | Privacy Policy
Standard Process sells exclusively through Health Care Professionals
© 2009 Standard Process Inc. All rights reserved.