This webinar will help you understand what a Quality Management System is in the context of clinical research, how to apply risk management concepts and strategies for implementing a risk based approach to fulfill your monitoring obligations.
Why Should You Attend:
If you interpreted the FDA’s Risk-Based Monitoring Guideline to mean that you do not need to visit research sites to accomplish your regulatory monitoring obligations, you may be partly right. The key to making centralized monitoring an acceptable alternative is to ensure that you are evaluating potential risks and addressing those risks within the context of your Quality System.
Official Website: http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702525?channel=yahooevent
Added by complianceonlinecom on October 19, 2012