Investigator Initiated Trials - What Are We Doing to Ensure Human Subject Protection? 2013

Topics

• Way to ensure human subject protections
• The importance of investigator-initiated trials
• What are the site responsibilities in investigator initiated trials
• The investigator deficiencies
• The resources available to help the investigator in the conduct of investigator-initiated trials
• The approaches or concerns of Institutional Review boards

Who should Attend

• Senior Clinical Research Associates(CRAs)
• Principle Investigators
• Contract Research Organizations (CROs)
• Clinical Research Project Manager
• Site Management Organizations (SMOs)
• Institutional Review Boards (IRBs)