| You are advised to take this training with the aid of printed handouts. Handouts, in pdf format, can be downloaded by clicking the hyperlink 'download' of each unit. The web pages are best viewed with Internet Explorer 5.5 or above in 1024 x 768 high colour and with full screen (function key F11). Loudspeakers are required. In addition to the pdf handouts mentioned above, you are also advised you to print out a copy of the ICH GCP E6 Guideline, the guideline adopted by our Research Ethics Committee (HKU/HA HKW IRB). |
| If you are a doctor or a nurse, would you like to register for CME/CNE points? | ||
| (Note: Points will be given to participants who have completed the Powerpoint presentations and taken the GCP examination.) |
| The Trial Landscape | Handout |
Duration (min:sec) |
| » Why Clinical Trials? | 18:07 |
|
| » Main Features of Clinical Trial Design | 27:15 |
|
| » The History of Clinical Trials | 17:12 |
|
| » The Drug Development Process | 23:16 |
|
| » Phases of Clinical Trials | 17:12 |
|
| » Clinical Trial Players | 18:25 |
|
| » Trial Guidelines - GMP, GLP and GCP | 19:53 |
|
| » Quality Assurance - Audits and Inspections | 13:52 |
|
| » Research Ethics | 24:17 |
|
| » Risks and Benefits of Trial Participation | 10:58 |
|
| » Sample Examination (12 multiple-choice questions) |
| Slides and script were developed by Professor J Karlberg and read by Mr. J Thorburn, Clinical Trials Centre (CTC), The University of Hong Kong. |