Unit-level history
Every pack, lot or part carries one ordered history from commissioning to dispense or installation.
One product. Many organizations.
A connected history from origin to destination.
Track medicine and critical goods through attested handoffs. Share provenance while protecting commercial terms.
Trace the journeyThe manufacturer creates the serial record. Each later handoff adds an attested link to this product’s history.
The manufacturer registers each pack or lot and attests to its origin. From that moment the unit has one history that everyone agrees on.
Every transfer must be attested by both sender and receiver. Price, quantity and terms are kept in a private collection shared only by those two partners and, where required, the regulator.
The logistics provider attests the temperature record for each shipment. Its fingerprint is tied to the custody event so it cannot be swapped later.
A pharmacy checks the pack before handing it to a patient: is it authentic, is it recalled, has it already been dispensed somewhere else?
The manufacturer or regulator flags a lot. Every later verification of an affected pack is refused across the whole network.
Every pack, lot or part carries one ordered history from commissioning to dispense or installation.
Both sides of every transfer sign it, so custody gaps and one-sided claims stand out immediately.
Prices and quantities live only in collections shared by the trading pair and any declared regulator.
A recall is a single attested event that every verification respects immediately.
Logger records are attested by the carrier and bound to the shipment they describe.
Regulators join as members of the collections they are entitled to inspect. That membership is public, so nothing is watched in secret.
Collection membership and attestation metadata are visible. Private payload access depends on the organizations declared in each collection.
| Information | Trading partners | Regulator | Other companies | Validators |
|---|---|---|---|---|
| Prices, quantities and terms | Yes | Where declared a member | No | No |
| Custody details of a transfer | Yes | Where declared a member | No | No |
| Pack status at verification | Yes | Yes | When verifying that pack | No |
| Recall notices | Yes | Yes | Yes | Yes |
| That each hand-off was attested by both sides | Yes | Yes | Yes | Yes |
The ledger verifies recorded claims and attestations. Physical authenticity and sensor accuracy still depend on the organizations and devices supplying the evidence.
Each action in the supply chain has an attestation policy committed to the ledger. Validators enforce it without ever seeing the commercial data behind the transfer.
Rules such as the US Drug Supply Chain Security Act and the EU Falsified Medicines Directive require pack-level tracking. But the partners who must share that data also compete with each other.
Pooling data in one platform exposes volumes, prices and customer lists to the operator, and sometimes to rivals.
When each company keeps its own records, a diverted or fake pack can re-enter the chain where no one is comparing notes.
Finding every affected unit means requests to each distributor, spreadsheets and days of uncertainty for patients.
Cold-chain logs are PDFs attached to emails. Proving a pack stayed in range is hard after the fact.
Compliance and brand protection without exposing distribution deals.
Meet traceability rules without handing volumes to competitors.
Authenticity, recall and duplicate-dispense status in one answer.
Declared access to the records you are entitled to, with full history.
Commercial details of a transfer are stored only in the collection shared by the two trading partners and any regulator declared as a member. Other companies can inspect membership and attestation metadata, but do not receive private prices, quantities or transfer documents.
Only the collections it is a declared member of. Membership lists are public on the ledger, so every company knows exactly what the regulator can inspect.
Yes. ChainOfCustody is designed to take events from existing serialization and warehouse systems through APIs, so staff keep using the tools they know.
The transfer is not complete until both sides attest. An unconfirmed hand-off is visible to the partners involved as an open item, which is exactly the gap traceability rules want surfaced.
Pharmaceuticals are the first focus because the rules are strict and the stakes are high. The same model fits medical devices, aircraft parts, food safety and battery passports.
Qkite is in active development with design partners.
Explore the protocol and the other applications built on it.