Clinical Trial auditing - Identifying risks and building a more compliant and successful trial

Learn how to successfully pass a clinical trial audit, how to prepare for it, where and how to identify the non compliance. Know FDA inspection strategy to identify areas of common deficiency.

Why Should You Attend:

With the growth of the Pharmaceutical and Biotechnology industry, audits get more and more frequent. Noncompliance in clinical trials and misreporting of clinical trial results that took place in the last years made the regulatory bodies to multiply the number of audits. On the other part, the sponsors also multiplied the audits from their part in the idea to try to downsize the risk of noncompliance during the trial.
This clinical trial audit webinar will help with preparing the site and the study team with how to successfully prepare for an audit, how to identify risk of noncompliance, what to do before, during and after an audit. The session will give you practical solutions to get the best results from an audit and the opportunity to grow the image of your team and/or your site. This session will include the key principles of audit preparation, GCP as defined by the ICH as well as incorporate FDA regulatory inspection strategy to identify areas of common deficiency.

Areas Covered in this Webinar:

• Key aspects of the role and key players involved in a trial.
• Understanding compliance.
• Most frequent audit findings.
• Audit preparation.
• Activities that are common to audits.
• Linking responsibility to these activities.
• Responding to audit findings.

Who Will Benefit:

This webinar will provide valuable assistance to all personnel in:

• Clinical trial sponsors study team
• CROs study team
• Study managers, Clinical team leads, CRAs
• Principal investigators, site managers and study coordinators
• Regulatory Compliance Associates and Managers