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

Venue: Online Event

Location: Palo Alto, California, United States

Event Date/Time: Sep 06, 2012 End Date/Time: Sep 06, 2012
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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.

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.


Online Event
2600 E. Bayshore Road
Palo Alto
United States