Clinical Trial Auditing - Identifying risks and building a more compliant and successful trial
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Clinical Trial Auditing - Identifying risks and building a more compliant and successful trial
Jul 12, 2012 - Jul 12, 2012
Event Type: Webinar
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Jul 12, 2012 8:00 - Jul 12, 2012 9:30
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Location: Online Event
Registration Deadline: None
Abstract Submission Deadline: None
Description of event:
This Clinical trial auditing training will provide an understanding of how to conduct compliant and successful clinical trials by defining FDA clinical trial audit procedures, audit program, audit planning and audit preparation.
Why Should You Attend: The field of GCP has rapidly evolved over the last few years and the requirements are getting tougher. Many companies find themselves unprepared for a clinical trial audit, either at a clinical site or their headquarters.
Areas Covered in the Seminar:
- What is clinical Audit?
- Audit Vs. Research.
- The Audit Cycle.
- Five stages of Clinical Audit.
- QA Program factors- implementing a program in place.
- What are the risks?
- What a sponsor and investigator need to know about FDA audit?
- Interactive case study to learn about audits.
- Tips for a successful study.
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