Archive: Phase I Study Management

April 11, 2014 | Barnett International Recording

Web Seminar Archives are available in either USB Flash Drive or DVD Format.

Archives are also available in SCORM format for LMS integration. Please contact Barnett at (215) 413-2471 for more details and pricing on SCORM files.

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$625.00

Course Description

Because the early life of a compound is dependent on the data and analysis derived from Phase I Studies, it is imperative that these trials are managed and conducted with the highest quality and care. Therefore, well-honed project management skills that can address the unique issues associated with Phase I Studies are needed. This web seminar will examine the importance of Phase I Studies in drug development, the issues commonly associated with conducting a Phase I Study from a sponsor perspective and provide project management best practices specific to overseeing a Phase I Study.

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Learning Objectives

  • Define Phase I Studies
  • Examine the importance of Phase I data in clinical development
  • Review general considerations for planning and conducting a Phase I Study
  • List project management best practices specific for Phase I clinical trials

Who Should Attend

  • Project Managers
  • Study Directors
  • Site Monitors

Instructor

The course will be led by one of the following instructors:

Linda Carter, R.N., B.S.N.

Click here for complete trainer biographies

 

Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.