In the past I have been responsible for picking lots to be placed on stability. Since AI can do a significant amount of management, a simple SOP update to transfer the planning responsibility over to the stability department would be the easiest path to mitigate missed stability protocol initiation and pulls. If your organization has such a flow, I would simply use the Sample Management “non-routine sample request” form to have Manufacturing ensure they pull the required vials to be put on stability.
As always, communication with the stability stake holders, i.e. manufacturing and manufacturing planners, QA and QC analytical departments, etc., is important to ensure you get your stability samples collected and set down according to protocol.
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This reply was modified 4 months, 3 weeks ago by joao4515.
