Audit/Inspection Preparedness for Clinical Research/Site Coordinators 2012 is a webinar that covers topics such as:
- Clinical Site Audits/Inspections findings and FDA warning letters
- Audits and Inspections: Definitions, Goals, Causes and Procedures
- Keeping site`s continuous Audit/Inspection preparedness
- Responsibilities of the Investigator and the clinical research coordinator
- Appropriate conduct during the Audit/Inspection
- Preparation for a planned Audit/Inspection
- DOs and DON`Ts prior to, during and after an Audit/Inspection
- Completion and follow up after the Audit/inspection
Audit/Inspection Preparedness for Clinical Research/Site Coordinators 2012 brings together Clinical Research Investigators, Clinical Research/Site Coordinators, Clinical Research / Project Assistants, Clinical Research Associates / Monitors, Clinical Team managers, Clinical Research Trainers, Regulatory Compliance Associates and Managers.
