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:
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.
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.
Date: September 06, 2012
Time: 10:00 AM-11:30 AM PDT
Cost: $199 per attendee per computer terminal
Registration: SIgn-Up on-line now. Add to your shopping cart.
Added by complianceonlinecom on August 8, 2012