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AHPA


AHPA Appoints Robert Wildman to Chair Sports Nutrition Committee

by Shari Barbanel | April 18, 2016

The American Herbal Products Association (AHPA) appointed Dr. Robert Wildman, chief science officer at Post Active Nutrition Brands, as the new chair of the Sports Nutrition Committee during a meeting at Natural Products Expo West in Anaheim, CA. Wildman succeeds Ray Jaglowski, vice president of technical and regulatory at Twinlab Corp., who chaired the committee ...

AHPA Advocacy Spurs Correction of FDA’s Dietary Supplement Labeling Guide

by Shari Barbanel | March 9, 2016

The U.S. Food and Drug Administration (FDA) has corrected its Dietary Supplement Labeling Guide after the American Herbal Products Association (AHPA) notified the agency of inaccurate information posted online. AHPA notified FDA in September 2015 that its guidance for industry titled “A Dietary Supplement Labeling Guide,” included one detail that contradicted current law and FDA regulations. ...

AHPA and UNPA Launch Campaign to Educate State AGs

by Shari Barbanel | January 27, 2016

The American Herbal Products Association (AHPA) and the United Natural Products Alliance (UNPA) have launched a joint campaign to develop working relationships with state attorneys general (AG) and educate them about the herbal supplement industry. This is the latest effort by AHPA and UNPA to ensure state AGs have an accurate understanding of the industry. ...

Frontline Segment: Skewed & Misleading, AHPA Says

by Shari Barbanel | January 20, 2016

A segment aired on January 19 on PBS’ Frontline presented dietary supplements as inherently unsafe by misrepresenting the rigorous safety provisions established for these products under the Federal Food, Drug and Cosmetics Act, the strict liability statute under which supplements are regulated. The segment, titled “Supplements and Safety,” relied on anecdotal reports of noncompliant products ...

FDA Updates Webpages to Reduce Confusion Between Legal Supplements and Illegal Drug-Spiked Products

by Shari Barbanel | December 7, 2015

The U.S. Food and Drug Administration (FDA) recently updated language on several pages of its website to more accurately describe illegal, drug-spike products and to remove references to these as dietary supplements after the American Herbal Products Association (AHPA) requested the changes. FDA usually uses terms such as “marketed as dietary supplements” or “masquerading as ...

DOJ Announces Supplement Sweep – CRN, NPA and AHPA Express Support

by Shari Barbanel | November 18, 2015

On Tuesday, November 17, Ben Mizer,  principal deputy assistant attorney general for the Civil Division of the Department of Justice (DOJ), revealed the government’s plan for a sweep of actions targeting unlawful dietary supplement makers and marketers. “We are here today to explain the critical steps the federal government is taking to stem the tide ...

Industry Involvement and Marketing

by Suzanne Shelton | September 1, 2015

2015 has been an extraordinarily challenging year for the dietary supplements industry, between legal challenges, scores of negative news reports, and substantial questions about industry practices from members of the U.S. Congress—and the year isn’t over. There are a lot of conversations taking place among members of the industry about what changes need to be ...

AHPA Proposal for Prop 65 Warning Gains Traction Among Regulators

by Angela Santoriello | October 2, 2014

In a breakthrough meeting with AHPA president Michael McGuffin, top officials of the California Office of Environmental Health Hazard Assessment (OEHHA) recognized the value of AHPA’s innovative proposal to allow more informative warnings for California’s Proposition 65-listed reproductive toxins to replace the inflammatory and alarming language currently required. Based on this understanding, OEHHA requested AHPA ...

AHPA Issues Cannabis Oversight Recommendations for Regulators

by Angela Santoriello | September 11, 2014

The American Herbal Products Association (Silver Spring, MD, AHPA) has published recommendations for regulators to address issues related to the safe use and responsible commerce of legally marketed products derived from Cannabis species. Several states, including Massachusetts, Oregon, Nevada, and Illinois have considered AHPA’s recommendations in the development of state medical marijuana program regulations and AHPA’s recommendations ...

New FDA Inspection Tips from AHPA

by Angela Santoriello | June 25, 2014

The American Herbal Products Association’s (AHPA) teleseminar played a large role in helping the dietary supplement industry recognize and observe good manufacturing practices. The two-hour teleseminar, held in the middle of May, had industry legal experts, including Justin Prochnow, Esq, Marc Ullman, Esq and Ashish R. Talati, Esq provide pertinent tips on U.S. Food and ...

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