Quality Assurance
Verification is the product
A research compound is only as useful as the documentation behind it. Every lot we release passes independent analysis before it reaches a laboratory.
Process
From synthesis to sealed vial
Five controlled stages, each documented and recorded against the batch number.
- 1
Synthesis & sourcing
Compounds are produced by vetted synthesis partners working to documented specifications, with raw-material traceability retained for every lot.
- 2
Independent HPLC analysis
Reverse-phase high-performance liquid chromatography confirms purity of ≥99% before a batch is cleared for filling.
- 3
Mass spectrometry identity check
Molecular weight is confirmed against the expected value to verify the correct sequence has been supplied.
- 4
Cleanroom filling & sealing
Vials are filled, stoppered and crimp-sealed under controlled conditions, then labelled with batch number and dosage.
- 5
Batch release & documentation
A Certificate of Analysis is issued and tied to the batch number printed on the vial, so results can always be traced back to the material in hand.
Testing standards at a glance
- Purity threshold
- ≥99% by HPLC
- Identity confirmation
- Mass spectrometry
- Testing cadence
- Every production batch
- Documentation
- Batch-matched Certificate of Analysis
- Storage on release
- -20°C, light protected