CLINICAL TRIALS CTR
| Researcher : Chan MY |
| List of Research Outputs |
| Chan M.Y., Facilitation of Site Monitoring, Audits and Inspections (Nov 2014), Training Workshop on GCP Trials Principles & Practice for Investigators & Clinical Research Personnel in China on Nov 29 - Nov 30, 2014. 二零一四年十一月二十九 日至三十日研究者與臨床 研究人員GCP試驗原則及 應用培訓工作坊, 2014. |
| Researcher : Lou KC |
| List of Research Outputs |
| Lou K.C., Facilitation of Site Monitoring, Audits and Inspections (Dec 2014), Training Workshop on GCP Trials Principles & Practice for Investigators & Clinical Research Personnel in China on Dec 12 - Dec 13, 2014. 二零一四年十二月十三日 至十四日研究者與臨床研 究人員GCP試驗原則及應 用培訓工作坊, 2014. |
| Lou K.C., Regulatory Compliance in Clinical Research, 2015 HA Symposium on Clinical Research Compliance. 2015. |
| Researcher : Ng CT |
| List of Research Outputs |
| Ng C.T., Clinical Trial Design & Statistical Methodology, 2015 HA Symposium on Clinical Research Planning. 2015. |
| Researcher : Tam SYM |
| List of Research Outputs |
| Tam S.Y.M., Clinical Trial Protocol Development - Essential Elements Highlight, 2015 HA Symposium on Clinical Research Planning on Feb 11, 2015. 2015. |
| Tam S.Y.M., Experience in Clinical Trials of Chinese Medicines, Seminar on Research and Development of Chinese Medicines 2014. 2014. |
| Tam S.Y.M., Quality Control for Sponsored and Investigator-initiated Clinical Studies, 2015 HA Symposium on Clinical Research Planning on Jan 29, 2015. 2015. |
| Researcher : Wong CKW |
| List of Research Outputs |
| Wong C.K.W., Clinical Research Ethics Guidelines, Symposium on Clinical Research and Research Ethics Evaluation. 2014. |
| Wong C.K.W., Clinical Research Ethics Review: Key Dimensions & Ethical Considerations; Facilitation of Initial Review; Facilitation of Continuous Oversight, 2014 HA Practical Workshop on Clinical Research Ethics Oversight & Research Ethics Committee Operations. 2014. |
| Wong C.K.W., HKU Clinical Trials Centre, Looking Backward, Moving Forward, The Regional East Asian Clinical Trial Annual Forum (REACTA). 2014. |
| Wong C.K.W., ICH GCP: Insight for Investigators & Study Site Personnel; Quality Management at Study Site; Safety Management and Reporting; Study Documents Management, Training Workshop on GCP Trials Principles & Practice for Investigators & Clinical Research Personnel on Aug 1, 2014. 2014. |
| Wong C.K.W., ICH GCP: Insight for Investigators & Study Site Personnel; Safety Management and Reporting; Study Documents Management; Study Planning; Facilitation of Site Monitoring, Audits and Inspections, Training Workshop on GCP Trials Principles & Practice for Investigators & Clinical Research Personnel in China on Dec 17 - Dec 18, 2014. 2014. |
| Wong C.K.W., ICH GCP: Insight for Investigators & Study Site Personnel; Safety Management and Reporting; Study Documents Management; Study Planning; Facilitation of Site Monitoring, Audits and Inspections, Training Workshop on GCP Trials Principles & Practice for Investigators & Clinical Research Personnel in China on Nov 22 - Nov 23, 2014. 2014. |
| Wong C.K.W., ICH GCP: Insight for Investigators & Study Site Personnel; Safety Management and Reporting; Study Documents Management; Study Planning; Facilitation of Site Monitoring, Audits and Inspections, Training Workshop on GCP Trials Principles & Practice for Investigators & Clinical Research Personnel in MENA. 2014. |
| Wong C.K.W., ICH GCP: Insight for Investigators & Study Site Personnel; Safety Management and Reporting; Study Documents Management; Study Planning, Training Workshop on GCP Trials Principles & Practice for Investigators & Clinical Research Personnel in China on Dec 13 - Dec 14, 2014. 2014. |
| Wong C.K.W., ICH GCP: Insight for Investigators & Study Site Personnel; Safety Management and Reporting; Study Documents Management; Study Planning, Training Workshop on GCP Trials Principles & Practice for Investigators & Clinical Research Personnel in China on Nov 29 - Nov 30, 2014. 2014. |
| Wong C.K.W., ICH GCP: Overview & Principles; ICH GCP: Insight for Investigators & Study Site Personnel; ICH GCP: The Roles of Sponsor-Investigator in Investigator-initiated Clinical Studies, 2015 HA Symposium on Clinical Research Ethics & Good Clinical Practice. 2015. |
| Wong C.K.W., ICH GCP: Overview & Principles; ICH GCP: Insight for Investigators & Study Site Personnel; ICH GCP: The Roles of Sponsor-Investigator in Investigator-initiated Clinical Studies, 2015 HA Symposium on Clinical Research Legal & Regulatory Affairs. 2015. |
| Wong C.K.W., ICH GCP: Overview & Principles; ICH GCP: Insight for Investigators & Study Site Personnel; Safety Management and Reporting; Study Documents Management, Training Workshop on GCP Trials Principles & Practice for Investigators & Clinical Research Personnel in China on May 9, 2015. 2015. |
| Wong C.K.W., Overview of Clinical Research Planning; Ethics Compliance in Clinical Research, 2015 HA Symposium on Clinical Research Planning. 2015. |
| Researcher : Yau HKC |
| List of Research Outputs |
| Yau H.K.C., Clinical Research Compliance; Clinical Research Ethics & International Guidelines; Research Ethics Committees: ICH GCP & Beyond, 2015 HA Symposium on Clinical Research Ethics & Good Clinical Practice on Feb 11, 2015. 2015. |
| Yau H.K.C., Clinical Research Compliance; ICH GCP: Overview & Principles; ICH GCP: Roles and Responsibilities of Sponsors & CROs; Informed Consent: Principles & Practical Considerations; Quality Assurance at Study Sites; Investigational Product Management, Training Workshop on GCP Trials Principles & Practice for Investigators & Clinical Research Personnel in China on Nov 22 - Nov 23, 2014. 2014. |
| Yau H.K.C., Clinical Research Compliance; ICH GCP: Overview & Principles; Informed Consent: Principles & Practical Considerations; Quality Assurance at Study Sites; Investigational Product Management, Training Workshop on GCP Trials Principles & Practice for Investigators & Clinical Research Personnel in China on Dec 13 - Dec 14, 2014. 2014. |
| Yau H.K.C., Clinical Research Compliance; ICH GCP: Overview & Principles; Informed Consent: Principles & Practical Considerations; Quality Assurance at Study Sites; Investigational Product Management, Training Workshop on GCP Trials Principles & Practice for Investigators & Clinical Research Personnel in China on Dec 17 - Dec 18, 2014. 2014. |
| Yau H.K.C., Clinical Research Compliance; ICH GCP: Overview & Principles; Informed Consent: Principles & Practical Considerations; Quality Assurance at Study Sites; Investigational Product Management, Training Workshop on GCP Trials Principles & Practice for Investigators & Clinical Research Personnel in China on Nov 29 - Nov 30, 2014. 2014. |
| Yau H.K.C., Clinical Research Compliance; ICH GCP: Overview & Principles; Informed Consent: Principles & Practical Considerations; Quality Assurance at Study Sites; Investigational Product Management, Training Workshop on GCP Trials Principles & Practice for Investigators & Clinical Research Personnel in MENA. 2014. |
| Yau H.K.C., Clinical Research Compliance; Informed Consent: Principles & Practical Considerations; Quality Assurance at Study Sites; Investigational Product Management, Training Workshop on GCP Trials Principles & Practice for Investigators & Clinical Research Personnel in China on May 9, 2015. 2015. |
| Yau H.K.C., Clinical Research Compliance; Informed Consent: Principles & Practical Considerations; Quality Assurance at Study Sites; Investigational Product Management, Training Workshop on GCP Trials Principles & Practice for Investigators & Clinical Research Personnel on Aug 1, 2014. 2014. |
| Yau H.K.C., Clinical Research Compliance; Research Ethics Committees: ICH GCP & Beyond, 2015 HA Symposium on Clinical Research Ethics & Good Clinical Practice on Jan 29, 2015. 2015. |
| Yau H.K.C., Clinical Research Governance: Practical Experience of HKU-CTC, Symposium on Clinical Research and Research Ethics Evaluation. 2014. |
| Yau H.K.C., Clinical Research in Hong Kong - and the Potential Development in the Private Healthcare Sector, The Hong Kong Doctors Union Symposium. 2015. |
| Yau H.K.C., Clinical Trials Management Experience in Hong Kong, Seminar of the 307th Hospital of Chinese People's Liberation Army. 2014. |
| Yau H.K.C., Hospital Governance System for Clinical Research Projects, Kiang Wu Hospital Symposium on Hospital Governance for Clinical Research. 2015. |
| Yau H.K.C., Informed Consent: Principles & Practical Considerations, HKU Research Integrity Symposium. 2015. |
| Yau H.K.C., Management of International, Multicentre, Investigator-initiated Clinical Studies, Hong Kong Paediatric Haematology & Oncology Study Group Monthly Scientific Meeting. 2015. |
| Yau H.K.C., Overview of Local Legal Requirements Applicable to Clinical Research; Personal Data Protection in Clinical Research; Informed Consent: Principles & Practical Considerations; Common Local Legal Issues in Clinical Research, 2015 HA Symposium on Clinical Research Legal & Regulatory Affairs. 2015. |
| Yau H.K.C., Professional REC Secretariat & Secretary; Evolution of Clinical Research Ethics; Establishment of Research Ethics Committees; REC Membership, SOP & Record Management; Reporting & Review of Safety Events in Clinial Trials, 2014 HA Practical Workshop on Clinical Research Ethics Oversight & Research Ethics Committee Operations. 2014. |
| Yau H.K.C., Risk Management & Insurance for Clinical Research, 2015 HA Symposium on Clinical Research Planning. 2015. |