NSF certified. cGMP compliant. FDA-registered. These aren't just labels — they represent the processes, documentation, and testing protocols that define how we manufacture every product that leaves our facility.
Download NSF Certificate (PDF)
NSF International is one of the world's most respected independent certification bodies for dietary supplements and food safety. An NSF Certificate of Conformity means a third-party auditor has verified that our quality management system, manufacturing processes, and documentation meet NSF's stringent requirements.
This certification is not self-reported — NSF conducts regular audits of our facility, reviews our batch production records, and tests finished products to confirm that what we say we do matches what actually happens on the production floor.
Current Good Manufacturing Practices are not optional for dietary supplement manufacturers. Here's exactly what we do to comply.
Every manufacturing step has a written Standard Operating Procedure. Our team follows these procedures every single run — not just during audits. SOPs cover equipment cleaning, weighing protocols, blending parameters, capsule filling tolerances, and release criteria.
All scales, meters, and measuring equipment are calibrated on a documented schedule. Calibration records are maintained as part of our Batch Production Records (BPR). Equipment that drifts out of tolerance is taken off-line immediately.
Each incoming raw material is tested for identity before use. We verify that what the supplier shipped matches what was ordered — by specification, COA, and in-house testing. Finished lots are tested for potency to confirm label claims are met.
Every batch receives a unique lot number that ties back to every raw material used, every test result generated, and every piece of equipment that touched it. If a supplier ever issues a recall, we can trace every affected product within hours.
All production and QA staff complete documented training on cGMP principles, cross-contamination prevention, personal hygiene, and their specific job procedures. Training records are maintained and reviewed during audits.
Our 20,000 sq/ft facility is designed for GMP compliance: segregated raw material and finished goods areas, controlled-environment encapsulation rooms, positive-pressure clean zones, and scheduled deep cleaning between production runs.
Title 21 of the Code of Federal Regulations, Part 111, is the FDA's Current Good Manufacturing Practice regulation for dietary supplements. It establishes comprehensive requirements for the manufacture, packaging, labeling, and holding of dietary supplement products.
Key areas covered by 21 CFR Part 111 include:
Compliance with 21 CFR Part 111 is enforced by FDA inspections. Our facility is FDA-registered and has been inspected without issuing significant observations.
Read: Quality Control in Supplement ManufacturingWe test before encapsulation and again after. No product is released without passing both stages.
Every incoming ingredient is quarantined until our QA lab runs identity testing (organoleptic and/or analytical). Supplier COAs are reviewed against our internal specifications. Any material that fails identity or does not match the COA is rejected and returned.
After precision blending, a sample is pulled and tested for homogeneity — confirming that all active and excipient ingredients are evenly distributed throughout the batch. This prevents hot spots and dose inconsistency.
We test for potency (active ingredient concentrations against label specifications) and screen for heavy metals and microbiological limits before any material enters the capsule filling equipment. Lots that fail do not proceed.
A statistically significant sample from each finished lot is tested for fill weight uniformity, dissolution characteristics, and a final potency confirmation. Weight variation must be within ±3% per capsule. Results are recorded in the Batch Production Record.
Only a qualified QA manager may authorize release of a finished lot. The release signature confirms all in-process and finished testing has passed, all documentation is complete, and the product meets every element of the approved specification.
Every released lot comes with a Certificate of Analysis summarizing testing results, raw material lot numbers, encapsulation date, and QA sign-off. You can present this COA to your customers, retail buyers, or regulatory reviewers.
Our NSF Certificate of Conformity is available for download as a PDF. Share it with your retail buyers, distributors, or customers who need proof of our quality credentials. The certificate includes our facility address, scope of certification, certificate number, and expiration date.
If you are a brand working with us and need additional quality documentation — such as facility registration, SOPs, or allergen statements — please contact us directly.
Our article on quality control in supplement manufacturing explains every stage of our QA program in detail — from raw material testing to lot traceability.
Our certifications are your assurance of quality. Contact us to discuss your product and request a free quote.
