Enhancing the Effectiveness of Serious Adverse Event Reporting in Clinical Trials: A Framework for Continuous Improvement

dc.contributor.advisorChaudhary, Pankaj
dc.creatorBonsu, Chelsea O.
dc.date.accessioned2024-01-24T22:23:30Z
dc.date.available2024-01-24T22:23:30Z
dc.date.issued2023-12
dc.format.mimetypeapplication/pdf
dc.identifier.urihttps://hdl.handle.net/20.500.12503/32465
dc.language.isoen
dc.subjectadverse events
dc.subjectclinical trials
dc.subjectquality
dc.subjectpatient safety
dc.subjectclinical research
dc.subjectsafety reporting
dc.subject.meshPatient Safety
dc.subject.meshClinical Protocols
dc.titleEnhancing the Effectiveness of Serious Adverse Event Reporting in Clinical Trials: A Framework for Continuous Improvement
dc.typeThesis
dc.type.materialtext
thesis.degree.departmentSchool of Biomedical Sciences
thesis.degree.disciplineClinical Research Management
thesis.degree.grantorUniversity of North Texas Health Science Center at Fort Worth
thesis.degree.nameMaster of Science

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