Regulatory
Non-GMO Tip 5: Non-GMO Verification for Better Business?
Companies must have a realistic understanding of the timeframes and effort involved.
What Actions Could FDA Possibly Take on Caffeine This Year?
The first months of 2015 have already offered the agency several possible opportunities to comment or take regulatory action on caffeine.
Going Non-GMO: Be Realistic-and Start Early
FDA Acts against Adulterant DMBA
The move comes less than a week after FDA enforced against a different stimulant adulterant.
Why Won’t NY Attorney General Schneiderman Release the Report? (Editorial)
No transparency? Pivotal data in the case building against the dietary supplement industry is still under the NY AG's lock and key.
Which Way to Quality Assurance?
The New York Attorney General wants better quality assurance for dietary supplements. So does the supplements industry. So how does it get there?
GNC CEO Encourages Supplements Industry to Embrace New Test Methods Like DNA Testing, Following NY AG Probe
GNC’s CEO Mike Archbold says industry “should embrace, not fear, novel testing methods.”
Stimulant Adulterant Still in Supplements for Weight Loss, Sports Performance, According to Study
FDA has drawn criticism for failing to act despite being aware of the adulteration.
NY AG Takes Dietary Supplements Fight to Congress
Attorney General Eric Schneiderman’s letter asks Congress to launch investigation on supplements.
Freedom to Operate
Nutraceutical companies who pursue IP litigation are protecting the industry at large.
NY AG, GNC Reach Agreement. But Is It a Mistake?
The Council for Responsible Nutrition says it is “disappointed” by the outcome: “We believe it’s a mistake.”
Folic Acid in the U.S. Threatened by Proposed Nutrition Label Changes?
While global health bodies emphasize the importance of folic acid, could proposed policy changes in the United States take us a step backwards?
Is GHRP the "New" Dietary Supplement Adulterant to Watch For?
While not necessarily “new,” growth hormone releasing peptides could become an “issue,” said John Travis of NSF International.
“All in One” Portal Will Help QA Managers Manage Non-GMO, Organic, and Kosher Certifications
The alliance could eventually include a centralized software platform that enables QA managers to manage multiple certifications.
Suppliers and Manufacturers Must Cooperate in Regulatory Compliance
Pending food manufacturing regulations mean manufacturers and suppliers must work together toward compliance.
DNA Experts Discuss What Makes Testing Difficult in NY AG Case
Experts in DNA testing have come together in a new white paper questioning proper use in the ongoing dietary supplement investigation led by NY AG Eric Schneiderman.
Making Algae Omega-3 Oil Work in Food and Beverage
Qualitas Health discusses pursuing GRAS affirmation for food and beverage use.
The Future of GRAS Regulations
What's changing? Industry initiative for enhanced self-regulation of GRAS practices is likely.
FSMA: What's Happening in 2015?
FDA’s Food Safety Modernization Act: 2014 actions and 2015 deadlines
Editor: New York Attorney General Case Requires Strong Response, Supplement Leaders Say
Will industry’s messaging be heard in the fight against New York Attorney General Eric Schneiderman?
Dietary Supplement Industry Issues in 2015
Key issues facing the natural products industry in 2015, according to Nutritional Outlook’s editorial advisory board.
Updated: Krill, Menhaden, and Salmon Oils Now Up for Inclusion in Codex Draft Standard
Krill, menhaden, and salmon oils (both farmed and wild)-which previously were excluded-will now be included in the draft standard.
Circuit Court Rules on POM Wonderful: A New Precedent for Disease-Related Claims?
Will one randomized controlled trial (RCT) become the new standard for any company making disease-related claims?
Senators Push for Powdered Caffeine Restrictions, CRN Applauds
The push for regulating the ingredient comes after two young men died from using powdered caffeine last year.
Latest Prop 65 Draft Leaves “Room for Improvement,” Says AHPA
Will the latest proposed revisions for Prop 65 actually lead to fewer lawsuits and more informed consumers?
How Does EFSA’s Caffeine Assessment Match Up with Other Global Standards?
The Council for Responsible Nutrition weighs in on a new caffeine assessment in Europe.
EFSA Says Caffeine Safe for EU Adults at 400 mg Daily or 200 mg in Single Dose
The EU opinion includes details on caffeine's combo with alcohol and exercise, plus safe doses for children.
CRN Foundation Pledges to Fund Supplement Advertising Watchdog NAD through 2017
The NAD self-regulatory program for the dietary supplement industry will continue for at least another three years.
New Law Lets U.S. DEA Crack Down on Steroid Supplement Spiking
DASCA enables DEA to more quickly classify designer anabolic steroids as controlled substances and to go after companies spiking.
Guide to Preventing Economically Motivated Food Fraud
The guide advises companies on steps to prevent economically motivated adulteration (EMA) at the ingredient level.