Quality Assurance at the (Clinical Research) Site: How to Develop a Manageable Plan

Why Should You Attend:

This webinar will show how you can develop a mechanism for providing feedback from QA to enhance education and training of your investigators and coordinators. If you belong to a site, or work with a site, that relies on external sources - monitoring visits, IRB review, FDA audit, etc. - for evaluation and feedback, then your site will benefit from this training.

In this 90-minute session, you will learn fundamental concepts and strategies to get your site started with a QA program that verifies clinical research practices as they are operationalized at the local site.

Learning Objectives:

At the end of this program attendees will be able to:

• Describe the purpose of a Site Quality Assurance Program.
• Differentiate a QA program, monitoring and auditing.
• Utilize resources to evaluate a clinical research program.

Areas Covered in the Seminar:

• Elements of  Quality Assurance Program.
• Elements of Monitoring.
• Elements of Auditing.
• Roles and responsibilities of study team members.
• Training and Education requirements.
• Implementing change.