Service

Supplement Testing

Full-spectrum testing for dietary supplements—potency verification, identity testing, heavy metals screening, and complete certificates of analysis. ISO 17025 accredited with 48–72 hour turnaround.

What We Test

Comprehensive testing to keep your products compliant, your labels accurate, and your brand protected.

Potency & Active Ingredient Analysis

Quantitative verification that your product contains what the label says it does. We test active ingredient concentrations against your label claims to ensure compliance with FDA regulations and consumer trust. If your potency numbers are off, you find out before your product ships—not after.

Active ingredient quantification
Label claim verification
Overage & degradation assessment
Multi-component formulation testing

Identity Verification

Confirm that your raw materials and finished products are exactly what they’re supposed to be. Identity testing is a cGMP requirement under 21 CFR 111 for dietary supplements, and we perform it using validated methods that satisfy FDA expectations and auditor scrutiny.

Raw material identification
Finished product verification
Botanical authentication
Spectroscopic & chromatographic methods

Heavy Metals Screening

Screen for arsenic, cadmium, lead, and mercury—the four heavy metals of greatest concern in dietary supplements. Contamination can come from soil, water, or manufacturing equipment, and even trace levels can pose health risks to consumers and regulatory exposure to your brand.

Arsenic (As) testing
Cadmium (Cd) testing
Lead (Pb) testing
Mercury (Hg) testing

Certificate of Analysis (COA)

Every test we perform results in a comprehensive Certificate of Analysis that documents methods used, results obtained, and pass/fail determinations against your specifications. Our COAs are designed to satisfy your internal quality teams, third-party auditors, and retail partners.

Full method documentation
Specification-based pass/fail
Digital images of results
Auditor & retailer ready

Why It Matters

Supplement testing isn't just good practice\u2014it's a regulatory requirement and a business necessity.

FDA cGMP Compliance

21 CFR Part 111 requires identity testing of every incoming raw material and appropriate testing of finished products. We help you meet these requirements with validated methods and complete documentation.

Retailer Requirements

Major retailers increasingly require third-party COAs from ISO 17025 accredited labs before accepting supplement products. Our testing satisfies Amazon, Walmart, and specialty retailer requirements.

Label Accuracy

The FTC and state attorneys general are actively pursuing supplement companies for label claim violations. Independent potency testing protects your brand from regulatory action and consumer lawsuits.

Ready to Test Your Products?

Ship your samples today. Results in 48–72 hours with complete COA.