Welcome to Veritacor Manufacturing
Texas-Based, Privately Held Leader in Nutraceuticals & Dietary Supplements. Veritacor is a Texas-based, privately held leader in cGMP certified and FDA-registered manufacturing of premium nutraceuticals and dietary supplements. Our state-of-the-art facility specializes in producing safe, effective, and compliant products for brands across the nation, all supported by rigorous third-party testing and a Certificate of Analysis to ensure transparency and quality. We offer custom formulation and private label supplement options, making us a trusted partner for brands seeking tailored solutions.
As an industry leader in the manufacturing of dietary supplements, Veritacor is committed to meeting the highest NSF and GMP standards. Our team provides end-to-end manufacturing services, from concept to packaging, ensuring your product is built with quality every step of the way.
Why Partner with Veritacor?
- FDA-registered, cGMP-certified facility for uncompromised quality
- Third-party tested products for reliability and consumer trust
- Texas-based facility with custom & private label manufacturing options
- Privately held with a commitment to innovation in nutraceuticals
Choose Veritacor, your Texas-based, trusted partner in the nutraceutical manufacturing industry, and see how we can help bring your supplement vision to life.
Our Services
We offer services in the manufacturing of
Powder Filling
Capsules
Uncoated Tablets
Packaging
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
finished products. - 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
Office Phone
830 875 5222
Location
1873 N. Magnolia Ave,
Luling Texas 78648
Office Hours
Mon - Thur: 7:30am - 6pm
Sat - Sun: Closed