Fundamentals of FDA’s Clinical Trial Audits – A Must- Know for Audit preparation

This Clinical Trial Audits webinar will provide help both CRAs and sites utilize quality improvement methods and effectively prepare for upcoming GCP audits.

Areas Covered in the Seminar:

• Differentiation of work of an auditor vs. Clinical Research Associate.
• Most common audit deficiencies noted among sites and sponsors.
• Techniques used in audit planning.
• Factors involved in selection process.
• Overview of GCP regulations and FDA guidelines used for audits.
• Audit documentation and proper follow-up procedures.

Overview of Preparing for Audit.

For More Details:
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