Qalitex Laboratories
Supplement and cosmetic testing lab covering identity, potency, pesticides and preservative efficacy.
- LEAD TIME
- 48 hours for standard panels
Overview
Qalitex Laboratories reports ISO/IEC 17025 accreditation for its dietary supplement, cosmetic, and consumer goods testing laboratory with facilities in Irvine and San Diego, California. Their A2LA accreditation scope covers identity, potency, heavy metals (ICP-MS), microbiology (USP methods), and pesticide testing for dietary supplements. Qalitex also offers preservative efficacy testing, stability studies under ICH guidelines, and regulatory compliance support. Testing programs are designed to meet 21 CFR Part 111, California Proposition 65, Amazon compliance, and Health Canada NHP Directorate standards. Standard panel turnaround starts at 48 hours. Qalitex publishes educational resources on ISO 17025 accreditation and independent lab testing, including a March 2026 guide for testing labs seeking accreditation.
Certifications
0 of 1 certification independently confirmed. What this means
Capabilities
- PRODUCT TYPES
- Identity Testing · Potency Testing · Heavy Metal Analysis · Microbiology Testing · Stability Studies
- CAPABILITIES
- Identity testing · Potency or label-claim testing · Heavy metals, pesticides, allergens or other contaminants · Microbiology testing · Stability (shelf-life) studies · Amazon compliance testing · Rush or fast turnaround
Sources
- Qalitex - About / ISO/IEC 17025:2017 Accreditation(2026-08-14)
- Qalitex - ISO 17025 Accreditation Achievement(2026-03-26)
- Qalitex - Independent Lab Testing Guide(2026-03-26)
What we couldn't verify
We did not visit this company on site. See the limits that apply to every listing.
- A2LA accreditation claimed but not found in A2LA public directory across three checks (April 4, April 6, April 7 — last check searched all 5 US accreditation bodies plus ILAC international signatories with 0 hits anywhere). 21 days after press release; possibly indexing lag, possibly registered under different legal entity name, possibly premature announcement. Re-check planned for April 16, 2026 (30 days post the March 17, 2026 press release date).
- California locations only (Irvine + San Diego)
- Amazon TIC status not assessed (Amazon publishes its approved-provider roster only inside Seller Central, which we cannot read)
- Contact information (email, phone) not publicly available
Dietary supplement manufacturers must comply with 21 CFR Part 111 (cGMP). What Part 111 requires
The connection map between Qalitex Laboratories and other vendors, capabilities, and certifications is in the manufacturer atlas.
Enforcement screening: included in Inventory Ready's most recent completed pass against FDA's published recall datasets (2026-07-09). Method and limits →
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