about
Designing an Adverse Drug Event Reporting System to Prevent Unintentional Reexposures to Harmful Drugs: Study Protocol for a Multiple Methods Design.Why Clinicians Don't Report Adverse Drug Events: Qualitative Study.Adverse Drug Event Reporting From Clinical Care: Mixed-Methods Analysis for a Minimum Required DatasetOrganizational implications of implementing a new adverse drug event reporting system for care providers and integrating it with provincial health information systems
P50
description
researcher
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wetenschapper
@nl
name
Serena S Small
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Serena S Small
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type
label
Serena S Small
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Serena S Small
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prefLabel
Serena S Small
@en
Serena S Small
@nl
P31
P496
0000-0003-3627-9042