- This topic has 3 replies, 3 voices, and was last updated 1 year, 6 months ago by .
I’m looking for some feedback on what everyone’s standard practice is in terms of drug accountability. If all drug is counted and verified at the clinical site before returning to a depot for destruction, do you also have the depot recount the drug in any fashion either down to the container level or down to the drug product unit?
Many thanks for your responses in advance!
You must be logged in to reply to this topic.