Audit/Inspection Preparedness for Clinical Research/Site Coordinators 2012
March 6, 2012(Ended)
Online Webinar
Audit/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.
Prices *
249-1099 US Dollar
Exhibition
No exhibition
Organization
Categories
Concurrent events
- Software Verification and Validation Planning and Implementation 2012
- When FMLA ends and ADA begins. The FMLA/ADA Crossover: Coordination, Management, and Compliance Strategies 2012
- Medical Device Adverse Event Reporting and Vigilance System During Clinical Trials and Post-Marketing: US, EU, and Canada 2012
Important
Please, check the conference website for possible changes, before you make any traveling
arrangements
* Prices are for evaluation only.
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