Documentation you can audit.
Six pillars of quality control. Nothing ships without full analytical verification.
Every batch ships with a full analytical report — HPLC purity, Mass Spec identity, and appearance.
USP <85> LAL endotoxin, sterility, and bioburden checks across the fill line.
USA-based synthesis partners audited annually against documented QMS controls.
We publish a strict ≥ 98% floor. Most batches exceed 99%.
A scannable batch ID on every vial ties directly to its full test panel and shipping record.
COAs and MSDS accessible in your customer portal for every historical batch.
From synthesis to bench.
A traceable chain of custody at every stage.
USA-based synthesis partner. Lot-level lineage recorded.
Third-party HPLC + Mass Spec. Retention samples archived 24 months.
LAL testing per USP <85>. Bioburden monitored across fill.
COA generated and attached to the batch record.
Insulated, temperature-controlled to your facility.
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