Sample Information
Product name, batch/lot ID as printed on the vial, sample form, submitter, date received, date tested, date issued, turnaround, and public listing status.
Verify published PacifiCOAnalytics results by report ID. Certificates include sample metadata, identity and purity, optional endotoxin and elemental impurities, method notes, and laboratory attribution. Corrections stay visible alongside the original.
Enter the report ID printed on the certificate (format PCA-2026-123456).
COAs are released after technical review. If a valid ID does not resolve, contact info@pacificoanalytics.ca with the ID and invoice number.
Aligned with our Certificate of Analysis layout (identity and purity, endotoxin, elemental analysis).
Product name, batch/lot ID as printed on the vial, sample form, submitter, date received, date tested, date issued, turnaround, and public listing status.
Peptide identity confirmed vs reference (FTIR-ATR, CE-UV, Raman, UV-Vis), purity as the main-peak area percentage, optional net peptide content - each with specification and status.
On full-panel reports: LAL kinetic endotoxin (EU/mg) and colorimetric screening for Pb, As, Cd, Hg with specification limits. Endotoxin methodology references USP <85> style principles.
PACIFICOANALYTICS INC. provides independent analytical testing of submitted samples for research and quality-documentation purposes only. Results apply only to the specific sample as received and do not certify remaining inventory or a production batch unless a documented sampling protocol was agreed in writing before intake. PacifiCOAnalytics has no ownership or vendor relationship with submitters and does not sell, manufacture, or distribute the materials tested. Results are not an evaluation of safety, efficacy, potency, sterility, or fitness for any use, are not medical, pharmaceutical, veterinary, or regulatory advice, and are not approval by Health Canada or the U.S. FDA. Materials tested are not evaluated for human or veterinary use, consumption, compounding, injection, or clinical practice. Any correction or re-test is published alongside the original, timestamped, and does not replace it. Services are provided as is. Liability is limited to fees paid for the specific test.