Bradford Williams appointed to lead dietary supplement GMP facility registration program.
Has FDA effectively slammed the door shut on DMAA?
Five dietary supplement associations sent new comments to FDA recently regarding the agency’s new dietary ingredient (NDI) draft guidance and NDI ingredient identity.
The FTC’s recent opinion in the POM Wonderful pomegranate case reveals more about the agency’s view on health-benefit claims.
A petition to FDA calls for nutrition label changes and more.
On behalf of the Truth in Advertising Campaign, Marc Ullman presented FTC with 26 non-compliant marketers of dietary supplements.
An official agreement will influence facility inspection rates between the United States and New Zealand.
Technical difficulties delayed public access to the renewal process, so FDA is offering a deadline extension.
Senators Durbin and Blumenthal finally got their meeting with FDA commissioner Margaret Hamburg.
Will a new, negative Department of Health and Human Services report follow the dietary supplements industry for years?
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