Quality assurance
Uncompromising standards. Every batch.
AVRL Aminos compounds are manufactured, tested, and verified to the highest research-grade specifications — so you can trust every vial, every time.
Enter your lot number to pull up the exact COA for your batch
Third-party verified
Lab Testing & Certificates of Analysis
Every compound is independently tested by a third-party laboratory. Browse all available COAs below — organized by product category.
GLP / Metabolic
3 recordsGrowth Hormone Peptides
7 recordsCJC-1295 + Ipamorelin
CJC-1295 No DAC
CJC-1295 With DAC
Ipamorelin
Ipamorelin
Tesamorelin
Tesamorelin
Tissue & Recovery
6 recordsBPC-157
BPC-157 + KPV
BPC-157 + TB-500 + KPV (KLOW)
KPV
TB-500
Wolverine (BPC-157 + TB-500)
Mitochondrial & Longevity
9 recordsKLOW
MOTS-C
MOTS-C
NAD+
NAD+
SS-31
SS-31
5-Amino-1MQ
5-Amino-1MQ
Skin & Cosmetic
6 recordsNeuro & Cognitive
5 recordsFOR RESEARCH USE ONLY. All COAs are issued by independent third-party laboratories. Documents are specific to the listed product and concentration. Batch/lot numbers are printed on each COA PDF — click "View COA" to see the full document including lot number, test date, and purity results.
Quality assurance
Uncompromising standards.
Every batch.
From raw material sourcing to final packaging, every step of our process is designed to deliver research-grade compounds you can trust.
Our commitments
Six pillars of quality
99%+ Purity Verified
Every AVRL compound is independently tested to confirm a minimum 99% purity threshold. We do not release a batch until it passes.
Third-Party Tested
All testing is conducted by accredited, independent laboratories — not in-house. No conflicts of interest. Just objective results.
USA Manufactured
Formulated and fulfilled from USA-based facilities operating under strict quality management systems and GMP-aligned practices.
Lot-Level Traceability
Every product carries a unique lot number traceable back to its raw material source, synthesis batch, and test results.
HPLC & MS Analysis
We use High-Performance Liquid Chromatography and Mass Spectrometry to confirm compound identity, purity, and concentration.
Cold-Chain Integrity
Temperature-sensitive compounds are stored and shipped under controlled cold-chain conditions to preserve stability and potency.
Testing scope
What we test for
Purity
≥99%
HPLC analysis
Identity
Confirmed
Mass spectrometry
Sterility
Tested
USP <71> method
Endotoxins
Tested
LAL assay
Residual solvents
Tested
GC-MS analysis
Heavy metals
Tested
ICP-MS screening
Step by step
Our quality process
From raw material to your door, every step is documented, tested, and verified.
Raw material sourcing
We source pharmaceutical-grade raw materials from vetted suppliers with documented purity certificates and chain-of-custody records.
Synthesis & formulation
Compounds are synthesized and formulated in USA-based facilities following GMP-aligned protocols with full batch documentation.
Independent lab testing
Each batch is sent to an accredited third-party laboratory for HPLC purity analysis, mass spectrometry identity confirmation, and sterility testing.
Certificate of analysis
A Certificate of Analysis (COA) is generated for every batch, documenting purity percentage, compound identity, test date, and lot number.
Quality release
Only batches that meet or exceed our 99%+ purity threshold and pass all identity and sterility checks are approved for release.
Fulfillment & cold-chain
Approved products are packaged under controlled conditions and shipped with appropriate cold-chain handling to preserve compound integrity.
See the Results for Yourself
AVRL is preparing an online library for product-specific Lab Testing and Certificate of Analysis documentation. Testing documentation will be added as it is received and verified.