Good Clinical Practices for the Clinical Research Professional
概览
Gain the basic knowledge required to conduct clinical trials, including information about subject safety, regulations, and the practicalities of performing research studies. Course Level: Beginner
内容纲要
Roles and responsibilities of each member of the study team
Regulations and guidelines that govern clinical investigations
Informed consent elements and processes
Successful patient recruitment and retention strategies
Adverse event handling and reporting
谁应该参加？
Clinical investigators
Clinical research professionals
Sub-investigators
Study staff
学习目标
At the conclusion of this activity, participants should be able to:
Identify the roles and responsibilities of each member of the study team including the clinical investigator, sub-investigator, study staff, IRB, and sponsor
Apply the regulations and guidelines for conducting safe and effective clinical trials
Describe the various processes for informed consent
Describe the requirements in reporting adverse events
