When cargo lands at Logan and moves to a regional depot for interim storage or last-mile coordination, it transfers to a party who often knows nothing about the shipment’s compliance history, temperature profile, or documentation requirements. That handoff is where chain-of-custody breaks.
For commercial pharmaceuticals, a documentation gap at a depot transfer can be remediated. For diagnostic reagents, biotech intermediates, and research samples, it frequently can’t.
A reagent that passes temperature review but fails documentation continuity can produce invalid test results — and the failure isn’t detected until the assay is complete. A biological intermediate whose transfer records are incomplete arrives at the next development stage without a defensible chain of custody. A research biospecimen that cannot demonstrate continuous documented custody from collection through receipt loses its regulatory standing, and no supply chain recovery plan replaces that.
The temperature record is necessary. It is not sufficient. For these material types, both records must be unbroken — and they must be held by the same operator, not assembled across parties after the fact.