Trial Master File (TMF) for Research Sites: Set Up and Maintenance October 2013

Oct 25, 2013
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Course Description

The investigator Trial Master File (TMF) is a collection of the essential documents for an investigator to record how they have fulfilled their regulatory obligations for a clinical trial project. This web seminar reviews the investigator TMF required and additional content for a clinical trial. The activities of set-up, maintenance, and quality control and assurance will be discussed along with common deficiencies and challenges.

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Learning Objectives

  • Discuss the changing regulatory climate and apply this to the essential documentation practices of an investigator of clinical trials
  • Examine the required components of an investigator TMF and recommend policy
  • Discuss maintenance and quality control of the TMF
  • Describe the Clinical Research Associate (CRA) contributions to and adequate monitoring of the investigator TMF

Who Should Attend

  • Research Site Personnel involved in the set-up and maintenance of any TMF or in charge of policy development and maintenance
  • Principle Investigators
  • Clinical Research Coordinators
  • Clinical Research Associate Managers
  • Clinical Research Associates
  • Quality Assurance Personnel of research sites and sponsors

Instructor

Gary B. Freeman, M.S., C.C.R.A.

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