Audit/Inspection Preparedness for Clinical Research/Site Coordinators 2012

March 6, 2012(Ended)
Online Webinar
Audit/Inspection Preparedness for Clinical Research/Site Coordinators 2012Audit/Inspection Preparedness for Clinical Research/Site Coordinators 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 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.

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249-1099 US Dollar
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Please, check the conference website for possible changes, before you make any traveling arrangements

* Prices are for evaluation only.