
GMP Harmonization: NSF Is Approved for Amazon Supplement Sales Rules
May 7, 2021
NSF independently registers manufacturers that meet GMP requirements. Registration services are available for manufacturers of dietary supplements, ingredients and raw materials, as well as distribution, warehousing and packaging companies that want to demonstrate a commitment to public health. NSF is committed to simplifying the auditing needs of every client, including retailers’ auditing needs through its GRMA certification programme.
Increase your company’s credibility and integrity and boost confidence in the preparedness of your facility for FDA inspection. Companies registered for GMP receive instant eligibility for entering products into NSF's product certification programme. These benefits extend to contract manufacturers registered for GMP through NSF, too. When your contract manufacturer is GMP compliant, you decrease the time and cost of NSF testing and product certification.
Our global network of auditors and technical staff is committed to helping your facility achieve GMP registration. Receive in-depth audit reports, thorough corrective action guidance and rapid responses to your questions.
With input from industry representatives, public health officials, regulators and consumer interest groups, NSF facilitated the development of the NSF/ANSI 455 GMP audit standards over the past five years.. We are currently transitioning clients from our GMP registration programme to the NSF/ANSI 455 GMP certification programme. This transition allows NSF to certify facilities to a consensus-based national standard and helps manufacturers reduce their annual audit burden.
We are currently accepting applications for audits for dietary supplements (NSF/ANSI 455-2), cosmetics and personal care products (455-3) and over-the-counter (OTC) drugs (455-4). The current dietary supplement GMP registration will be phased out entirely by 2022.
Both registration and certification provide leading GMP audits for dietary supplements, cosmetics and OTC drugs based on current Good Manufacturing Practices and federal regulations for each scope. For manufacturers, the key features NSF/ANSI 455 GMP certification provides in addition to GMP registration are: