Vial-to-COA Traceability

Scan the vial. Match the batch. Verify the independent record.

Each applicable Transition Biotech research-material vial carries a QR code and batch number that connect the physical vial to its independent Kovera Labs analytical record. This lets the recipient verify the vial against the laboratory record instead of relying only on a seller-hosted copy.

How vial-to-COA verification works

  1. Locate the vial QR code and batch number. Use the identifiers printed on the physical vial.
  2. Scan the QR code. The unique code opens that record on the independent Kovera Labs website.
  3. Match the batch. Confirm that the vial batch number agrees with the third-party report.
  4. Review the reported testing. Evaluate the identity, report number, methods, results, certification date, and documentation limits.

Why the batch match matters

A report applies to the sample and batch identified in that report. A product name, purity percentage, or seller-hosted PDF alone does not establish that a different vial belongs to the tested batch. The vial QR destination and matching batch number provide the verification path for the individual unit.

The public Transition Biotech page is a searchable transcription and convenient copy. The original Kovera Labs record and the identifiers printed on the vial remain the controlling evidence.

Search the published batch records

Search all batch COA records View the COA Library

10 independently verifiable research-material records are currently published.

Documentation boundaries

These records document the tests and results stated by the issuing laboratory for the identified sample. They do not establish clinical safety, efficacy, suitability for human or veterinary use, or results for an unmatched batch. Transition Biotech materials are supplied solely for lawful laboratory research.