Training on Current ICH GCP Guidelines 2013

Topics

• Coverage of ICH requirements for the Investigator, the sponsor and IRBs
• Background information on the need for standardized GCP guidelines for the clinical research industry
• Subject rights
• Informed consent
• What is an essential document?
• What is an adverse event?
• Retention requirements

Who should Attend

• Research Nurses
• Principal Investigators
• CRAs
• Study Coordinators
• Healthcare professionals needing to acquire documentation of current ICH GCP training
• Quality Assurance