Universal BioLabs is a U.S.-based manufacturer of research-grade peptides and bioregulators. We supply research laboratories, academic institutions, and biotech organizations with analytically verified compounds produced under strict quality-controlled manufacturing processes.
Every batch we produce is independently tested by three certified third-party laboratories before release. No batch ships without full analytical confirmation.
Researchers receive complete documentation with every order, including Certificates of Analysis (COA), HPLC purity reports, and LC-MS molecular confirmation data. We believe verification shouldn’t be optional — it should be the baseline.
All products are intended exclusively for in vitro laboratory research and are not for human consumption.
We exist to support serious research — not to cut corners, not to make claims, and not to ship unverified compounds.
Our mission is to provide laboratories and qualified researchers with the highest-purity, independently verified peptides and bioregulators available, backed by the analytical documentation to prove it.
Scientific progress depends on compound reliability. A result is only as trustworthy as the material behind it. That’s why we hold every batch to the same uncompromising standard: 99%+ purity, triple-verified by independent labs, with full documentation available before you place your order.
Universal BioLabs manufactures all compounds in U.S.-based facilities operating under strict quality-controlled production standards. Our process follows rigorous chain-of-custody protocols from raw material sourcing through synthesis, testing, and final packaging — every step documented, every handoff tracked.
Before any batch is approved for release, it undergoes a full analytical battery conducted by three independent certified laboratories:
Purity Verification — High-Performance Liquid Chromatography (HPLC) confirms ≥99% purity on every batch. No batch ships below threshold. No exceptions.
Molecular Identity Confirmation — Liquid Chromatography-Mass Spectrometry (LC-MS) verifies that the compound is exactly what the label states — correct molecular weight, correct structure.
Sterility & Endotoxin Testing — Ensures compounds meet research-grade sterility standards and are free from bacterial endotoxin contamination.
Contaminant Screening — Tests for residual solvents, heavy metals, and chemical impurities that could compromise experimental integrity.
Three labs. Four tests. Zero ambiguity.
Transparent Documentation
We publish full Certificates of Analysis for every batch — not behind a support ticket, not on request, not after purchase. They’re available now.
Review complete lab results, HPLC chromatograms, and LC-MS data before you order at: universalbiolabs.com/coa-library/
Universal BioLabs is one of the few research peptide suppliers that independently verifies every batch through multiple certified laboratories. This isn’t a marketing claim. It’s an auditable process with published results.
Our Testing Standards
Every compound must pass the following quality control benchmarks before it is approved for release. These are not guidelines — they are minimum requirements. A failure on any single parameter holds the entire batch.
Identity Confirmation — Analytical testing must confirm that the compound conforms to the labeled peptide. If the molecular identity doesn’t match, the batch is rejected.
Purity — Every batch must meet or exceed 99% purity as determined by HPLC analysis. We don’t publish a range. We publish a floor: ≥99%. One standard, applied universally.
Net Content — Vial content must fall within ±5% of the stated amount. What the label says is what the vial contains.
Endotoxin Testing — Bacterial endotoxin levels must test below 0.5 EU/mg or 5 EU per vial, in accordance with USP <85> (Bacterial Endotoxins Test). Endotoxin contamination can compromise cell-based assays and in vitro research outcomes — we test to ensure it doesn’t.
Sterility — Every batch must pass USP <71> (Sterility Test). Total Aerobic Microbial Count (TAMC) and Total Yeast and Mold Count (TYMC) must both fall within acceptable limits. No microbial contamination. No exceptions.
Heavy Metals & Residual Contaminants — Screened for heavy metal residues, residual solvents, and chemical impurities that could introduce experimental variables or compromise result integrity.
Documentation isn’t something we provide on request. It’s included, automatically, with every order, for every compound:
Certificate of Analysis (COA) — Batch-specific testing summary from each independent laboratory, including pass/fail status on all parameters above.
HPLC Purity Report — Full chromatogram data showing peak purity, retention times, and any detected impurities at the sub-1% level.
LC-MS Molecular Confirmation — Mass spectrometry data verifying the compound’s molecular weight matches the expected structure. This is how you confirm the vial contains exactly what it should.
Researchers can access the complete analytical dossier for any compound at any time, before or after purchase at universalbiolabs.com/coa-library/
