Identity & Potency
HPLC/UPLC, HPTLC
Confirms correct species/actives and verifies label claims for vitamins, botanicals, enzymes, and amino acids.
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Identity, potency, purity, and safety are the four pillars of supplement testing. From raw-material intake to release and shelf-life, our lab work is engineered to uphold these pillars before your product ships. We pair in-house screens for speed with ISO/IEC 17025 third-party lab confirmations for credibility, so you meet specs, retailer policies, and label claims without surprises
Every batch moves through a defined test plan—core safety and identity panels for all products, plus risk-based add-ons driven by your formula, claims, and channel.
HPLC/UPLC, HPTLC
Confirms correct species/actives and verifies label claims for vitamins, botanicals, enzymes, and amino acids.
ICP-MS
Pb, Cd, As, Hg against internal spec, retail thresholds, and Prop 65 exposure limits.
TAMC/TYMC
Total counts, yeast/mold, and absence of E. coli, Salmonella, S. aureus; probiotic products follow product-appropriate limits.
ELISA/PCR
Validates “free-from” statements and sanitation between allergen runs.
GC-MS
Verifies extraction/granulation solvents meet ICH Q3C limits.
LC-MS/MS
Multi-residue screens prioritized for botanicals and “organic” claims.
ICH-style
Room/accelerated to support shelf-life, potency retention, and USP performance tests (e.g., disintegration).
USP 2040/701
Confirms release characteristics for tablets/caps; critical for “fast-acting” or enteric claims.
KF/LOD
Prevents caking and microbial growth in powders/chews; supports packaging selection.
LC-MS/MS
Risk-based for botanicals and grains; needed for certain retail programs.
LC-MS/MS
Targeted screens for WADA-banned or undeclared actives in sports products.
qPCR
Additional identity confirmation where morphology is insufficient.
We prioritize ISO/IEC 17025–accredited third-party labs for identity, potency, safety, and claim substantiation using USP/AOAC methods.
Panels are scoped by risk and claims:
Chain-of-custody, controls, and reference standards are documented by the lab and mirrored in our LIMS. Final COAs tie to your batch record, streamlining retailer approvals and certification submissions.
We qualify ISO/IEC 17025-accredited laboratories by method, matrix, and turnaround, then route your products to the best-fit partner.
We align pull-points with your master batch record so testing supports speed and release confidence.
Yes—dietary ingredients are 100% identity-verified. Additional purity/contaminant tests are added based on risk and channel.
For accreditation, specialized methods, certification programs, or retailer submissions. We pick the best-fit lab for the matrix and method.
Yes. We align the proper ELISA/PCR, identity, and pesticide/GM screens, then coordinate with certifiers as needed.
Yes. We verify inputs and run targeted assays (e.g., porcine DNA screens if required) through qualified partners, then package documentation for your certifying body.
Yes—through NSF Certified for Sport® and Informed Sport partners, including lot-by-lot testing where programs require it.
We run indicative or ICH-style stability based on risk and claims, then trend potency and micro to justify dating.
We default to USP/AOAC where available. When no compendial method exists, our partners use validated, fit-for-purpose procedures with full validation summaries on request.
We apply risk-based ICP-MS and, if you sell in California, compare exposures to Prop 65 levels. We can help set warning label triggers or engineer formulas/servings below thresholds.
From Amazon and retail specs to sports and practitioner claims, we coordinate ISO 17025 third-party reports tied to your lots. We’ll build the plan and handle the paperwork, no busywork on your side.