Quality & Manufacturing

Testing architecture
that holds up to scrutiny

We don't perform our own purity testing and report it on a COA. Every lot is submitted to an accredited third-party analytical laboratory with no commercial interest in the result. The COA attached to your order is their report, not ours.

A compound isn't verified because a supplier says so. It's verified when an independent laboratory confirms purity, identity, and endotoxin levels against a defined specification — and the data is attached to a lot number you can trace.
Arcovex Quality Standard · Applied to every lot before release
Testing methods applied per compound profile
HPLC
High-Performance Liquid Chromatography
Primary purity quantification method. Separates compound from impurities by elution profile and quantifies each fraction by UV absorbance area.
Release threshold ≥98.0% area
LC-MS
Liquid Chromatography–Mass Spectrometry
Molecular identity confirmation. Verifies exact monoisotopic mass and fragmentation pattern against reference standard. Identifies sequence-level deviations.
Release criterion Identity confirmed
LAL
Limulus Amebocyte Lysate (Endotoxin)
Quantitative endotoxin detection using the LAL kinetic turbidimetric method. Applied to compound classes where endotoxin presence is a relevant analytical concern.
Release threshold <1.0 EU/mg
SDS
Safety Data Sheet
GHS-compliant safety documentation covering hazard classification, handling procedures, storage requirements, disposal guidance, and emergency response information.
Standard GHS Rev. 9
Batch verification & release flow
01
Synthesis & Manufacture
Contracted synthesis partner produces compound to specification. Internal QC hold applied. Lot number assigned.
QC Hold
02
Sample Submission
Representative sample submitted to accredited third-party laboratory. Chain of custody documented.
In Transit
03
Independent Testing
HPLC, LC-MS, and (where applicable) LAL endotoxin testing performed. Results reviewed against Arcovex release specifications.
Testing
04
Review & Release Decision
Passing lots receive a verification ID and COA. Lots failing any specification are rejected and destroyed.
Decision
05
QR Label & Record Index
Lot indexed to the Arcovex Verified record structure. Label printed with QR, lot, expiration, and purity summary.
Released

No lot enters active inventory without a passing third-party analytical report. This is not an internal quality assurance process — the testing laboratory has no commercial interest in the outcome and operates independently of Arcovex Biotech.

View Arcovex Verified →
Raw analytical data
Raw chromatogram files and source analytical data may be available upon request for a given lot, in addition to the summary COA.
Request Raw Data →