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Published in 2022 at "Pharmacoepidemiology and Drug Safety"
DOI: 10.1002/pds.5434
Abstract: Monitoring for substandard medicines by regulatory agencies is a key postāmarket surveillance activity. It is important to prioritise critical product defects for review to ensure that prompt risk mitigation actions are taken.
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Keywords:
risk classification;
substandard;
classification model;
prioritising management ... See more keywords