Trial Master File for Research Sites: Can You Pass FDA Inspection? 2011

  • 03 Aug 2011
  • Webinar

Description

Trial Master File for Research Sites: Can You Pass FDA Inspection is a webinar that covers topics such as:

  • Trial Master File (TMF) order is crucial for passing an FDA inspection
  • Documents for a Trial Master File
  • Create a compliant and useful TMF
  • Quality control and Maintenance of the TMF
  • CRA contributions and monitoring of the investigator TMF
  • Note to File (NTF)


Trial Master File for Research Sites: Can You Pass FDA Inspection brings together Clinical Research Coordinators, Clinical Research Managers, Clinical Trial Investigators and Clinical Research Associates.

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Important

Please, check "Trial Master File for Research Sites: Can You Pass FDA Inspection?" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations
Health & Medicine: Medical device, Medical laboratories, Pharma
Science: Biochemistry, Chemistry, Life Sciences & Biology
Technology: Biotechnology

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