Quality Systems
Quality is a system, not a slogan
Research depends on materials that are what they claim to be. Our quality system applies consistent, documented criteria to every lot before it reaches the catalog.
Acceptance Criteria
What every lot is measured against
Six criteria define whether a lot is released. Each is verified and recorded.
Identity
Mass spectrometry confirms molecular identity against the expected structure for each compound.
Purity
HPLC quantifies purity against a defined threshold, targeting ≥ 99% for released lots.
Content
Net peptide content is verified so documented quantities reflect what is delivered.
Stability
Lyophilized presentation and cold-chain handling preserve integrity from release to receipt.
Traceability
Every lot carries a unique number linking the product to its certificate of analysis.
Consistency
The same acceptance criteria are applied to every production lot, batch after batch.
The Process
From compound to catalog
A transparent, documented pathway. Nothing reaches the catalog without passing each stage.
Compound Selection
Source materials are selected against strict identity and quality criteria before intake.
Laboratory Analysis
Independent labs verify identity, purity, and content by HPLC and mass spectrometry.
Documentation
A batch-specific Certificate of Analysis is generated and archived by lot number.
Research Availability
Verified lots are released to the catalog with full documentation attached.
Every claim is backed by a document you can inspect.
Explore certificates of analysis by lot number, or request the documentation relevant to your research.