
Principle 11: Investigational products
Learn how ICH E6(R3) establishes comprehensive requirements for investigational product manufacturing, handling, storage, and documentation to ensure participant safety and trial integrity.
Principle 11: Investigational products
In a Phase III cardiovascular trial, a site pharmacy received a shipment of investigational product on a Friday afternoon. The receiving technician noticed the temperature monitor indicated the shipment had exceeded the upper storage limit during transit, but the excursion was brief—only 42 minutes above threshold. Uncertain whether this mattered, and with the pharmacist already gone for the weekend, the technician logged the shipment into inventory and placed it in the storage unit. The following Monday, when the pharmacist reviewed the records, the affected units had already been dispensed to three participants.