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Conference Directory
Do you have a GCP compliant Trial Auditing System/Process in place? - Risks & Rewards
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Venue Name: Online Event
Country: United States of America
City: Palo Alto
State: california
Number of Attendees: Unknown
Webinar or Virtual Event: Yes
Keywords: Clinical Development, Clinical Trial staff and management, Clinical Trial Auditing System, FDA clinical trial, clinical trial audit procedures, audit program, audit planning, audit preparation
Start Date of Conference:: 11-18-2011
End Date of Conference: 11-18-2011
Description of Conference: 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:
- QA Program factors- implementing a program in place.
- What are the risks?
- What a sponsor and investigator need to know about FDA audit.
- What is reviewed at the audit.
- Tips for a successful study.
- Preparing for a site visit.
- Most common FDA violations/actions.
NOTE : Use this Promocode (128600) to avail 10% discount, valid upto 16th November 2011.
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Do you have a GCP compliant Trial Auditing System/Process in place? - Risks & Rewards
