Query
A question raised about a data point in a CRF, which may or may not result in a correction. Note: this may also refer to
August 31, 2022
Quality Overall Summary (QOS)
The Quality Overall Summary (QOS) is a summary of all quality-related information provided by applicants to regulators in drug marketing or licensing applications
May 6, 2022
Qualified Person Responsible For Pharmacovigilance (QPPV)
An individual, usually an employee of a pharmaceutical company, who is personally responsible for the safety of the human pharmaceutical products marketed by that company
May 6, 2022

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