Quality Assurance at the (Clinical Research) Site: How to Develop a Manageable Plan December 6, 2012

This 90-minute webinar will show how you can develop and implement a Quality Assurance (QA) program at your clinical research site that ensures the staff are properly trained and that the research is carried out in accordance with regulatory expectations.

Why Should You Attend:

Is your site carrying out clinical research in accordance with regulatory expectations? You have training requirements for investigators and coordinators, is that enough? Is it worthwhile training that covers necessary topics? A Quality Assurance (QA) Program is the vehicle to help you answer these questions and more.

Quality assurance is often confused with monitoring or auditing. Understanding the principles of quality assurance and how QA differs from monitoring and auditing is critical to establishing a program that enhances compliance without creating unnecessary redundancy.

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.

Who will Benefit:

This webinar will provide valuable assistance to all personnel in:

- Experienced Clinical Research Coordinators
- Experienced Principal Investigators
- Experienced Clinical Research Associates (Monitors)
- Site Based Clinical Research Managers and Administrators
- Regulatory Compliance Associates and Managers

Official Website: http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702406?channel=yahooevent