|
|
 |
|
Viewing report
|
|
|
|
E-Learning Module: Roles and Responsibilities Under ICH GCP
CompuPharma Ltd
This CompuPharma Clinical Trial Module is ideal for people who are involved in Clinical Trials, from trial design to trial participation. The Module describes the roles and responsibilities of the different parties involved in initiating, conducting and overseeing clinical trials according to ICH Good Clinical Practice
Objectives:
- Define the principles of ICH GCP
- Describe the role and responsibilities of the investigator
- Describe the role and responsibilities of the sponsor
- Describe what is meant by informed consent
- List the responsibilities of an Independent Ethics Committee/Institutional Review Board
- Name the main parties involved in clinical trials
This is a self paced highly visual interactive e-Learning Module, with a full audio voiceover, which can be taken online. It has a 16 question multiple choice Assessment which the Trainee can perform once they have completed the module. For the Certified option, a hard copy certificate is mailed to the Trainee, once they have achieved a score of 100% in their Assessment.
|
|
|
|
