Quality Lab

Trust, but Verify. Then Verify Again.

Third-Party Verification

Independent laboratories validate what our in-house testing confirms.

Testing Panel

What We Test on Every Batch

Identity

PASS
Confirms raw material is exactly what the supplier claims. No substitutions, no adulteration.
Method: HPLC / FTIR / Microscopy Std: USP / AOAC

Potency

PASS
Validates active ingredient concentration matches label claims within specification.
Method: HPLC / UV-Vis Std: USP / EP

Purity

PASS
Screens for impurities, degradants, and residual solvents to ensure product safety.
Method: HPLC / GC Std: ICH Q3

Heavy Metals

PASS
Tests for lead, arsenic, cadmium, and mercury at parts-per-billion sensitivity.
Method: ICP-MS Std: USP <232>/<233>

Microbial

PASS
Total plate count, yeast & mold, E. coli, Salmonella, and Staph. aureus screening.
Method: Plate Count / PCR Std: USP <61>/<62>

Allergens

PASS
Screens for major allergens including soy, dairy, gluten, tree nuts, and shellfish.
Method: ELISA / PCR Std: FDA FALCPA

Certificate of Analysis (COA) issued for every production lot. Available upon request for international supplement trade, regulatory submissions, and customer verification.

Laboratory Testing

Why Third-Party

Independence Removes Bias

Our in-house lab catches issues fast. Third-party labs confirm we caught everything. This dual-layer approach is why brands trust Albert Max for verified pure ingredients and export-quality vitamins manufactured in California.

  • ISO 17025 accredited partner laboratories
  • Duplicate sample retention for dispute resolution
  • Results available within 5-7 business days
  • Digital COA delivery for fast international clearance

Transparency is Our Standard

Every claim we make can be verified. Every test result documented.

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