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Conference Paper: Clinical Research Compliance; ICH GCP: Overview & Principles; Informed Consent: Principles & Practical Considerations; Quality Assurance at Study Sites; Investigational Product Management

TitleClinical Research Compliance; ICH GCP: Overview & Principles; Informed Consent: Principles & Practical Considerations; Quality Assurance at Study Sites; Investigational Product Management
Authors
Yau, HKC
Issue Date2017
Citation
Training Workshop on GCP Trials Principles & Practice for Investigators & Clinical Research Personnel in China, 21-22 October 2017 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/299388

 

DC FieldValueLanguage
dc.contributor.authorYau, HKC-
dc.date.accessioned2021-05-11T10:16:23Z-
dc.date.available2021-05-11T10:16:23Z-
dc.date.issued2017-
dc.identifier.citationTraining Workshop on GCP Trials Principles & Practice for Investigators & Clinical Research Personnel in China, 21-22 October 2017-
dc.identifier.urihttp://hdl.handle.net/10722/299388-
dc.languageeng-
dc.relation.ispartofTraining Workshop on GCP Trials Principles & Practice for Investigators & Clinical Research Personnel in China-
dc.titleClinical Research Compliance; ICH GCP: Overview & Principles; Informed Consent: Principles & Practical Considerations; Quality Assurance at Study Sites; Investigational Product Management-
dc.typeConference_Paper-
dc.identifier.emailYau, HKC: kcyau@hku.hk-
dc.identifier.hkuros307499-

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