USP <2750> Manufacturing Practices for Dietary Supplements
Issued by United States Pharmacopeia (USP)
StandardAudit Scope
Provides good manufacturing practice (GMP) guidance for dietary supplements, including personnel, facilities, equipment, production controls, quality controls, and recordkeeping. Aligns with but does not duplicate 21 CFR Part 111.
What It Proves
A manufacturer has adopted USP's voluntary GMP guidance for dietary supplements as an internal quality framework.
What It Does Not Prove
USP <2750> is GUIDANCE, not certification. 21 CFR Part 111 is the LEGAL MANDATE for dietary supplement GMP; <2750> is supplementary best-practice text. There is no USP-issued <2750> certificate. Third-party GMP audits (NSF, NPA, SQF) are the independent verification mechanism for GMP claims.
How Vendors Report It
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