An Overview of Risk Management and Risk Analysis Techniques in Clinical Trials (Clinical Compliance)

Venue: Online Event

Location: Palo Alto, California, United States

Event Date/Time: Jul 26, 2012 End Date/Time: Jul 26, 2012
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Why Should You Attend:

If you are currently involved in clinical trials either as a CRA, project manager, investigator or sponsor, this webinar will provide you with an overview of risk factors in clinical trials and possible ways to mitigate, control, assess impact, and prevent them in your trial. We would discuss the key elements of risk management such as planning, identification, quantification, action, measurement, outcome assessment, and post-implementation review of various types of risks. Also discussed will be best practices for risk analysis and prospective planning in the project plan. At the end of the course, you would be able to review your current project plan for potential issues or help address these factors in the future clinical trial project plans that you may create.

If you are aspiring to be a clinical project manager, are sponsoring a clinical trial, supervise clinical trial operations, or would like to become a clinical site, this course is a must for you.


Online Event
2600 E. Bayshore Road
Palo Alto
United States