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Conference Paper: How to Ensure Adequate Adverse Event Reporting from Investigator/Clinical Trial Oversight Perspective

TitleHow to Ensure Adequate Adverse Event Reporting from Investigator/Clinical Trial Oversight Perspective
Authors
Yau, HKC
Issue Date2018
Citation
The 10th DIA China Annual Meeting, Beijing, China, 23-25 May 2018 How to Cite?
DescriptionClinical Development: Session 0406 - Clinical Trial AE Reporting—from Collection, to Processing, Analysis and Summary, to Authority Review
Persistent Identifierhttp://hdl.handle.net/10722/283795

 

DC FieldValueLanguage
dc.contributor.authorYau, HKC-
dc.date.accessioned2020-07-06T02:17:18Z-
dc.date.available2020-07-06T02:17:18Z-
dc.date.issued2018-
dc.identifier.citationThe 10th DIA China Annual Meeting, Beijing, China, 23-25 May 2018-
dc.identifier.urihttp://hdl.handle.net/10722/283795-
dc.descriptionClinical Development: Session 0406 - Clinical Trial AE Reporting—from Collection, to Processing, Analysis and Summary, to Authority Review-
dc.languageeng-
dc.relation.ispartofThe 10th DIA China Annual Meeting-
dc.titleHow to Ensure Adequate Adverse Event Reporting from Investigator/Clinical Trial Oversight Perspective-
dc.typeConference_Paper-
dc.identifier.emailYau, HKC: kcyau@hku.hk-
dc.identifier.hkuros700003856-

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