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UPCOMING LIVE SEMINARS
 
Monitoring Clinical Drug Studies: Beginner
August 26-28, 2014
Philadelphia, PA
Clinical Project Management: Advanced
September 10-11, 2014
San Diego, CA






Risk-Based Site Monitoring September 2011

Course Description

In the current GCP regulatory climate, risk-based decision making should be supported within the clinical Quality System. A management approach used in many industries where performance is critical under tight timelines for regulated activities, risk-based decision making makes sense for such activities as sponsor monitoring in clinical research. Applying a risk-based approach to the monitoring and site management should be based on a given project’s risk profile. A risk-based approach can address current monitoring practices that are costly and ineffective, and help projects meet financial and compliance goals. This web seminar will present the concepts and case scenarios of risk-based monitoring (RBM).

VideoPreview

 

Learning Objectives

  • Recognize where risk-based decision making fits into the clinical quality system
  • Identify risks for a project related to monitoring
  • Identify components to include in building the project profile risk score
  • Apply risk factors to various study decisions, i.e., monitoring plan, site assignments, and frequency

Who Should Attend

  • Site Research Managers
  • Clinical Research Associates/Monitors
  • Study/CRA Managers
  • Sponsors/CROs

Instructor

Sandra “SAM” Sather, M.S., B.S.N., C.C.R.A., C.C.R.C.

Click here for complete trainer biographies 

Course Length Time

1.5 hours; 12:00 – 1:30 p.m. Eastern

Course Dates

September 27, 2011

Hold this course at your company! For more information, contact Naila Ganatra at (215) 413-2471.