Key Aspects of the Trial Master File and How to Pass FDA Inspection - Webinar By GlobalCompliancePanel 2011

  • 03 Nov 2011
  • Webinar

Description

Key Aspects of the Trial Master File and How to Pass FDA Inspection is a webinar that covers topics such as:

  • Role and responsibilities of clinical trial staff
  • ICH guidelines and Good Clinical Practice (GCP)
  • Understanding compliance
  • Key aspects of the Trial Master File
  • Audit preparation
  • Most frequent audit findings
  • Developing a CAPA
  • Responding to audit findings

Key Aspects of the Trial Master File and How to Pass FDA Inspection brings together CROs Study Team / Study Managers, Clinical Trial Sponsors Study Team, CRAs, Clinical Team Leads, Site Managers and Study Coordinators, Principal Investigators, New Principal Investigators, New Clinical Research Coordinators, Regulatory Compliance Associates and Managers.

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Important

Please, check "Key Aspects of the Trial Master File and How to Pass FDA Inspection - Webinar By GlobalCompliancePanel" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Healthcare, Hospitals & Clinics, Medical device, Medical laboratories, Pharma

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