1
Document
Business credentials, catalogue data, recent batch COAs, fulfilment details and commercial terms are collected.
Quality framework
Evidence before catalogue claims.
Our launch framework is designed around batch traceability and documentation review. It is a commercial quality policy, not a claim of regulatory approval or suitability for human use.
Supplier documentation
- Legal business identity and fulfilment origin
- Batch or lot identification
- Certificate of Analysis linked to the supplied batch
- Purity data, preferably chromatographic
- Identity evidence, preferably mass spectrometric where relevant
- Storage and stability information where available
Catalogue controls
- Research-use-only classification
- No therapeutic or dosing claims
- Batch-level documentation references
- Supplier and product traceability retained internally
- Documentation review before commercial listing
- Complaint and batch investigation recordkeeping
Qualification sequence
How a supplier reaches the catalogue.
2
Review
Documentation is checked for batch specificity, test method clarity and alignment between identity, purity and lot records.
3
Approve
Only approved materials move to an active catalogue. Future batches remain subject to documentation checks.