Known origin
Manufacturer and manufacturing site must be identified beyond reseller branding.
Acceptance framework
Material standards.
The minimum evidence and governance conditions required before a material can be represented in the Notes for Innovation research catalogue.
Batch-linked evidence
COA and analytical records should map to the exact original lot.
Access control
Intended use and jurisdiction must be reviewed before any supply pathway is activated.
Minimum acceptance gate
Five things must be true.
Manufacturer is identified
Not merely a marketplace seller or private-label name.
Original lot is preserved
Internal relabeling must not erase source traceability.
Analytical evidence is batch-specific
Generic marketing certificates do not satisfy the evidence model.
Chain of custody is understandable
Manufacturer → exporter → intermediary → importer must be reconcilable.
Jurisdiction has been reviewed
No automatic assumption that “research only” resolves medicinal-product regulation.