Supplier infrastructure
Submit and manage your batch documentation records.
PurityLedger gives research compound suppliers a hosted batch record infrastructure — QR-verifiable pages, CoA fingerprints, conservative review statuses and a transparency profile without becoming a sales channel.
Onboarding workflow
4-step documentation setup
📋
01
Create supplier profile
Register your organisation, documentation workflow and lab partnerships on PurityLedger.
📄
02
Upload batch documentation
Submit CoA PDFs, batch numbers, test dates, and test method details for review.
🔬
03
Attach lab metadata
Link your third-party analytical lab results. PurityLedger records method, date and fingerprint.
✅
04
Publish QR batch record
Once reviewed, your batch gets a QR-verifiable public record with conservative status labelling.
Documentation submission
Submit batch for documentation review
Submit your batch documentation for review. This is a documentation submission — not a product listing, sale request, or regulatory filing.
Recent submissions
Pending documentation submissions
sub-001
BPC-157 (Research Reference)
Supplier: Aurora Research Materials · Batch: AR-BPC157-0626
Submitted: 2026-05-30
sub-002
Semaglutide Analogue (Research Reference)
Supplier: Nova Synthesis Registry · Batch: NV-SEMA-0526
Submitted: 2026-05-29
Awaiting third-party lab confirmation from Rhein MassSpec
sub-003
Selank (Research Reference)
Supplier: Cascade Analytical Registry · Batch: CA-SEL-0626
Submitted: 2026-05-22
Documentation complete; batch record created as PL-CA-260516-ENDO09
sub-004
Epithalon (Research Reference)
Supplier: Baltic Peptide Documentation Co. · Batch: BP-EPI-0526B
Submitted: 2026-05-27
Batch number format does not match supplier registration. Please resubmit with corrected format BP-[COMPOUND]-MMYY.
PurityLedger provides documentation review, batch record hosting, CoA verification tools and analytical testing coordination only. PurityLedger does not certify any product as safe, effective, legal, approved, or suitable for human or veterinary use. Testing records are batch-specific and do not constitute medical advice, regulatory approval, or endorsement of any supplier or product. Clients and users are responsible for compliance with applicable laws in their jurisdiction.