File Download

There are no files associated with this item.

Supplementary

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

TitleClinical Research Compliance; Informed Consent: Principles & Practical Considerations; Quality Management at Study Sites; Investigational Product Management
Authors
Issue Date2018
Citation
Professional Research Accreditation for Clinical Trials Investigative Site Executives (PRACTISE) Workshop, Hong Kong, 11 August 2018 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/299387

 

DC FieldValueLanguage
dc.contributor.authorYau, HKC-
dc.date.accessioned2021-05-11T09:58:19Z-
dc.date.available2021-05-11T09:58:19Z-
dc.date.issued2018-
dc.identifier.citationProfessional Research Accreditation for Clinical Trials Investigative Site Executives (PRACTISE) Workshop, Hong Kong, 11 August 2018-
dc.identifier.urihttp://hdl.handle.net/10722/299387-
dc.languageeng-
dc.relation.ispartofProfessional Research Accreditation for Clinical Trials Investigative Site Executives (PRACTISE) Workshop-
dc.titleClinical Research Compliance; Informed Consent: Principles & Practical Considerations; Quality Management at Study Sites; Investigational Product Management-
dc.typeConference_Paper-
dc.identifier.emailYau, HKC: kcyau@hku.hk-
dc.identifier.hkuros307514-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats