Third-party tested. Fully documented.
Every batch is HPLC purity tested by a third-party testing facility in the GTA. Endotoxin testing is carried out in addition to purity, and each batch below shows its own endotoxin status — PASS where results are complete, PENDING where testing is still in progress. Verifiable results with direct links to the testing facility.
Endotoxin relevance depends on the application: it matters for cell-culture and in vivo research, and is generally not a factor in analytical or chemical work. Purity, endotoxin clearance and sterility are separate measurements — one result is not evidence of another.
Each report covers only the sample sent to the lab, tested by the method shown. It doesn't describe any other vial, lot or batch.
A report is an analytical result. It isn't a judgement on safety, effectiveness or suitability for human or animal use, and it isn't medical advice.
For research use only · Not for human or veterinary use
NAD+ 1000 mg
Report #VDIC-NAD+-1000-091426
CJC-1295 10 mg
Report #VDIC-CJCN-10-100526
ARA 290 10 mg
Report #VDIC-ARA-10-101326
TB-500 10 mg
Report #VDIC-TB500-10-110326
5-Amino-1MQ 50 mg
Report #VDIC-5AM-50-101526
Cartalax 20 mg
Report #VDIC-CART-20-100626
BPC-157 10 mg
Report #VDE-BPC-10-070626
DSIP 10 mg
Report #VDE-DSIP-10-070626
GHK-Cu 100 mg
Report #VDE-GHK-Cu-100-071326
SEMA 20 mg
Report #VDE-SEMA-20-070626
RT 20 mg
Report #VDE-RETA-20-081726
RT 10 mg
Report #VDE-RETA-10-050426-02
KPV 10 mg
Report #VDE-KPV-10-052926
GLOW Blend 70 mg
Report #VDE-GLOW-70-052926
Epithalon 10 mg
Report #VDE-EPI-10-052926
Selank 10 mg
Report #VDE-SEL-10-052926
TIRZ 10 mg
Report #VDE-TIRZ-10-060826
KLOW Blend 80 mg
Report #VDIC-KLOW-80-110326
Tesamorelin 10 mg
Report #VDE-TESA-10-052926
Semax 10 mg
Report #VDE-SEMAX-10-052926
Ipamorelin 10 mg
Report #VDE-IPA-10-070626
Melanotan 2 10 mg
Report #VDE-MELA-10-070626
What's in a COA?
Our Certificates of Analysis include the following data from independent third-party testing:
High-performance liquid chromatography results confirming peptide purity ≥98%.
Unique batch identifiers, test dates, and laboratory information for full traceability.
Bacterial endotoxin levels measured via Kinetic LAL assay. Results are documented in the batch COA where this test was performed.
