Quality
Quality shouldn’t require trust. It should provide evidence.
Regent Peptides prioritises documented product verification, batch identification and independent analytical testing. Every stage of handling is recorded so that a compound can be traced from incoming material through to the documentation supplied with it.
Four stages, every batch
01
Source
Raw material sourced against defined identity and quality criteria, recorded against the incoming consignment.
02
Manufacture
Synthesis and lyophilisation carried out under controlled UK manufacturing conditions with batch records.
03
Analyse
Independent analytical testing by third-party laboratories using chromatographic and mass spectrometric methods.
04
Verify
Batch identification applied and quality documentation compiled prior to release for research supply.
What the documentation covers
- Identity
- Confirmation that the material corresponds to the stated compound.
- Purity
- Quantified analytical result for the tested batch.
- Method
- The analytical technique applied, typically HPLC with mass spectrometry.
- Batch reference
- The identifier printed on the product label.
- Form
- Lyophilised powder, sealed vial.
- Intended use
- Laboratory research use only.
Look up a batch reference
Analytical documentation is indexed by product and batch number. Search the record set to view what is available for your vial.
Open lab reportsFor research use only. Not for human consumption.