VERITACOR, LLC, is a Texas based, privately held leader in third party contract manufacturing for the nutraceutical and dietary supplement industry.
We offer services in the manufacturing of
What is GMP registration?
Good Manufacturing Practices (GMPs) are guidelines that provide a system of processes, procedures and documentation to assure a product has the identity, strength, composition, quality and purity that appear on its label. These GMP requirements are listed in Section 8 of NSF/ANSI 173 which is the only American National Standard in the dietary supplement industry developed in accordance with the FDA’s 21 CFR part 111.
NSF International independently registers manufacturers as meeting GMP requirements. The program is open not just to manufacturers of dietary supplements but also to manufacturers of ingredients and raw materials, as well as distribution, warehousing and packaging companies, who want to demonstrate their commitment to public safety.
Independent registration from the global public health organization demonstrates a commitment to dietary supplement quality and compliance with U.S. GMP requirements.
What does it take to be NSF GMP registered?
NSF GMP registration verifies that the facility that is audited twice annually for quality and safety in compliance with Federal Regulations for dietary supplements good manufacturing practices.
Good Manufacturing Practices (GMP) registration including:
- Audits of all production facilities that manufacture, package, warehouse
or distribute dietary supplements or functional foods
- Review of quality control testing procedures for raw materials and
- Review of maintenance, housekeeping, cleaning and sanitization
procedures Review of sourcing and traceability procedures
- Review of training and qualification programs Review of internal SOPs
- Product Recall Procedures