Third-Party Testing & Certificates of Analysis
Verification Status
This page reflects our current third-party verification standards, including recently updated batch-level testing, endotoxin screening, and printed batch traceability on all products.
All Certificates of Analysis (COAs) are independently hosted by the testing laboratory and can be verified directly at the source.
Canadian Independent Third-Party Testing
Each Certificate of Analysis reflects the specific batch submitted for testing and is used to support identity verification, purity confirmation, and batch-level traceability. As of our latest production cycle, batches now include printed batch numbers on vial labels, allowing direct correlation between the physical product and its corresponding test documentation.
Endotoxin Testing
As part of our most recent quality control upgrade, endotoxin testing has been introduced across all product batches. This additional layer of verification is designed to complement standard purity analysis and provide a more complete assessment of batch quality.
Current Batch Third-Party Testing & Verification
Current verified batches are listed below. Each entry identifies the tested batch and available purity and endotoxin results. Depending on the laboratory, purity and endotoxin testing may appear on a single Certificate of Analysis or on separate laboratory reports.
5-Amino-1MQ – 50 mg
Batch: MQ50-001 Purity: 99.49% Endotoxin: < 0.125 EU/mL
BPC-157 – 10 mg
Batch: BPC-013 Purity: 100.00% Endotoxin: < 0.125 EU/mL
CJC-1295 No DAC – 10 mg
Batch: CJC-016 Purity: 99.5% Endotoxin: Pending
View COA · View Endotoxin Testing
Epitalon – 50 mg
Batch: ET50-001 Purity: 99.03% Endotoxin: < 0.125 EU/mL
GHK-Cu – 50 mg
Batch: GHK-015 Purity: 98.8% Endotoxin: < 0.11 EU/mg
View COA · View Endotoxin Testing
GHK-Cu – 100 mg
Batch: CU1-014 Purity: 99.53% Endotoxin: < 0.125 EU/mL
Ipamorelin – 10 mg
Batch: IP-IPA-012 Purity: 99.76% Endotoxin: Not reported on current COA
Kisspeptin – 10 mg
Batch: KS10-001 Purity: 99.91% Endotoxin: < 0.125 EU/mL
KLOW – 80 mg
Batch: KLO-002 Purity: 98.71% Endotoxin: < 0.125 EU/mL
KPV – 10 mg
Batch: KPV-003 Purity: 99.8% Endotoxin: < 0.11EU/mg
View COA · View Endotoxin Testing
Melanotan II – 10 mg
Batch: MT2-012 Purity: 99.89% Endotoxin: < 0.125 EU/mL
MOTS-c – 10 mg
Batch: MS10-014 Purity: 99.0% Endotoxin: Pending
View COA · View Endotoxin Testing
MOTS-c – 40 mg
Batch: MS40-004 Purity: 99.5% Endotoxin: Pending
View COA · View Endotoxin Testing
NAD+ – 500 mg
Batch: NAD-001 Purity: 97.86% Endotoxin: < 0.125 EU/mL
PT-141 – 10 mg
Batch: PT10-002 Purity: 99.42% Endotoxin: < 0.125 EU/mL
Retatrutide – 10 mg
Batch: RT10-014 Purity: 99.81% Endotoxin: < 0.125 EU/mL
Retatrutide – 15 mg
Batch: RT15-014 Purity: 99.42% Endotoxin: < 0.125 EU/mL
Retatrutide – 20 mg
Batch: RT20-004 Purity: 99.3% Endotoxin: Pending
View COA · View Endotoxin Testing
Selank – 10 mg
Batch: SK10-002 Purity: 99.06% Endotoxin: < 0.125 EU/mL
Semax – 10 mg
Batch: SX10-001 Purity: 99.69% Endotoxin: < 0.125 EU/mL
SS-31 – 50 mg
Batch: SS50-001 Purity: 99.92% Endotoxin: < 0.125 EU/mL
TB-500 – 10 mg
Batch: IP-014 Purity: 99.22% Endotoxin: < 0.125 EU/mL
Certificates of Analysis shown correspond to current or most recent batches. If you require documentation from previous batches, please search our Historical COA Database.
Historical Certificates of Analysis
Looking for testing documentation from a previous batch? Our Historical COA Database provides a permanent archive of Certificates of Analysis from past Integrity Peptides product batches as newer batches replace them.
Historical records include available batch-specific third-party testing documentation, such as identity and purity analysis, measured vial content, and endotoxin testing where applicable. Maintaining these records allows researchers to review previous testing results and trace historical batches alongside our current Certificates of Analysis.
View the Historical COA Database →
Ongoing Independent Verification Practices & What to Expect:
Our objective is to maintain a continuously verified product line through independent, third-party testing conducted on a rolling batch basis. As new batches are produced, they are regularly submitted to qualified Canadian analytical laboratories to ensure ongoing consistency, accuracy, and transparency. Recent upgrades to our verification process include batch-level traceability through printed vial labels, expanded endotoxin testing protocols, and continuous alignment between tested samples and current inventory.
As additional testing is completed, new Certificates of Analysis will be published on an ongoing basis and linked directly to corresponding product listings. This ensures that available documentation reflects the most recent verified batches, rather than outdated or generic test results. Our approach is simple, we publish what has been tested, update as new data becomes available, and maintain a clear, verifiable record of product quality over time.
Our commitment to transparency:
We do not publish test results before they exist, and we do not overstate testing claims. This page exists to clearly communicate what documentation is currently available, what is in progress, and what will be published next.
COA Availability & Documentation Requests:
All Certificates of Analysis are batch-specific and reflect the exact material submitted for independent third-party testing. Current testing documentation is published alongside the corresponding product, while previous batch records are maintained within our Historical COA Database as newer batches replace them.
If you are looking for verification related to a specific product or batch, you are welcome to contact us directly. We’re happy to help identify the appropriate Certificate of Analysis, clarify current or historical testing status, and provide available supporting documentation where applicable.
Research use only:
All products are sold for research and laboratory use only. Certificates of Analysis reflect the specific sample tested and are provided for informational transparency only. Not for human or veterinary use.
