Index/Topics/Good Manufacturing Practices

Good Manufacturing Practices

Regulations for the manufacture of dietary supplements.

Fact-Checks

5 results
Jan 11, 2026
Most Viewed

How can consumers verify FDA facility registration and GMP certification for dietary supplement manufacturers?

Consumers can confirm that a dietary supplement facility is supposed to be registered with FDA because owners/operators of places that manufacture, process, pack, or hold supplements for U.S. consumpt...

Jan 11, 2026
Most Viewed

What regulatory steps should consumers take to verify safety and ingredient doses in cognitive supplements?

Consumers seeking to verify the safety and ingredient doses in cognitive supplements should treat products as post-market items that require detective work: read the Supplement Facts and label claims,...

Feb 5, 2026

How does the FDA regulate claims and safety reporting for dietary supplements marketed as weight‑loss aids?

The treats —including products marketed for —under a food-based framework established by , which means they generally do not require premarket approval for safety or efficacy and are regulated differe...

Jan 18, 2026

What regulatory steps are required before a drug like ART26.12 can enter commercial manufacturing and distribution?

A drug such as ART26.12 cannot move from laboratory success to commercial shelves without meeting a sequence of regulatory gates: demonstration of safety and efficacy through preclinical and clinical ...

Jan 15, 2026

What regulatory checks and manufacturing standards reduce contamination risk in commercial gelatin supplements?

Commercial gelatin supplements reduce contamination risk through a combination of regulatory frameworks (FDA oversight of dietary supplements, specific CFR rules for manufacturing, and recordkeeping f...