3x Tested Means Zero Compromises
Every ingredient. Every product. Verified for purity, potency, and contaminants—because your brand's reputation depends on it.
What drives us? Not the volume of products we produce—but the quality standards behind every single one.
From the moment raw materials enter our facility to the moment finished products arrive at your warehouse, we follow rigorous quality control protocols at every phase. Our passion isn't just in what we make. It's in how we make it.Pharmaceutical-Grade Standards. Total Peace of Mind.
In today's competitive marketplace, protecting your brand is everything. That's why we produce all our products using pharmaceutical-grade standards—higher than what's required for nutritional supplements. These strict guidelines aren't mandated by law. We follow them because they make our products superior and give our partners something rare: complete confidence.
Unmatched quality. 3-Phase Testing.
Every raw material is screened before it enters our facility. Contaminants are caught at the door—not in your products.
Phase 1
Incoming raw testing material
Identity
To confirm the ID of a given Raw Material and the accuracy of the Certificate of Analysis (COA) we use FTNIR (near infrared technology).
Purity
Vendor COA claims are checked for purity by HPLC, GC or ICP.
Heavy metals
We test for Arsenic, Cadmium, Lead and Mercury. Heavy Metals must be under the USP specified guidelines.
Microbial
We test for Total Plate count, Total Yeast and Mold count and Coliform bacteria to make sure that the Raw Material complies with the USP, AHPA and FDA guidelines.
Pathogens
Raw Materials are tested for E. coli, Salmonella, and Staphylococcus aureus pathogens (as needed).
Drug screen
Raw Materials are tested for banned steroidal substances (as needed).
Phase 2
During production testing
Cleanliness
We perform ATP swab tests prior to batch production and allergen swab tests as needed to ensure equipment is free of potential contamination or microbes.
Identity check
We use FTNIR to confirm the ID of a given in-process mix to ensure it contains the correct raw ingredients.
Purity check
Purity is checked by using HPLC, GC, and/or ICP to ensure the in-process mix will create a final product that meets label claims.
Phase 3
During production testing
Identity check
We use FTNIR to confirm the ID of a Finished Product.
Purity (label claim)
We check the purity by HPLC, GC, and/or ICP if there is a label claim on the Finished Product COA.
Microbial check
We test for Total plate count, Total Yeast and Mold count and Coliform bacteria to make sure that the Finished Product complies with specifications.
Pathogens check
We test again for the following pathogens, E. coli, Salmonella, and Staphylococcus aureus (as needed).
Allergen
We list the allergens, if present in the Finished Product.
Heavy metals check
We test the Finished Product for Heavy Metals contaminants (Arsenic, Cadmium, Lead and Mercury) and make sure they are under the USP specified guidelines.
Drug screen check
We use an outside 3rd party laboratory to conduct GC-MS/ HPLC-MS testing on finished products for banned steroidal substances, if needed.
What This Means for Your Brand
100%
of all inbound raw materials meet or exceed FDA standards
100%
of your finished products meet or exceed FDA standards
100%
of your finished products always meet label claims
Now that you understand what real quality requires… can you really afford to trust your next project to anyone less?