DSHEA

New and Upcoming FDA Changes in 2025: GRAS Rules, FOP Labelling, and Supplement Ingredients – What You Need to Know

16

Sep

0 Comments

FDAcanadian regulations, cross-border compliance, dietary supplements, DSHEA, FDA, FDA Unified Agenda, food labelling, FOP labelling, front-of-package labelling, GRAS, health canada, ingredient safety, NHP, nicotinamide mononucleotide, NMN, novel foods, Nutrition Labelling, Regulatory Affairs, self-affirmed GRAS, U.S. regulations

New and Upcoming FDA Changes in 2025: GRAS Rules, FOP Labelling, and Supplement Ingredients – What You Need to Know

On September 4, 2025, the U.S. Food and Drug Administration (FDA) published its Unified Regulatory Agenda, a key planning document that outlines the Agency’s top priorities over the coming year. Among the many proposed and final rules, three initiatives stand out for their potential to significantly impact food and dietary…

Read More

5 Dietary Supplement Violations and How to Avoid Them

11

Jan

0 Comments

UncategorizedBatch Production Records, Consumer health risk, Dietary Supplement Health and Education Act, dietary supplements, DSHEA, False advertising, FDA, FDA warning letters, GMP, Good Manufacturing Practices, The Food and Drug Administration, US dietary supplements

5 Dietary Supplement Violations and How to Avoid Them

With a projected U.S. market size of over $300 billion by 2030, the dietary supplement category has never presented more opportunities for brand success. In a health-conscious society, dietary supplements can play a significant role in supporting individuals' well-being, but the growing popularity of these supplements has brought attention to the…

Read More