Who Will Benefit

The TMF Institute’s professional development is for representatives from pharmaceutical, biotechnology, and medical device organisations as well as CROs and eTMF/TMF service providers having or seeking responsibilities following areas:

  • TMF/eTMF Systems Management
  • Clinical Document Management
  • Clinical Trial Documentation
  • Clinical Trial Administration
  • Clinical/TMF Project Management
  • Quality Control/Quality Management
  • Clinical Operations
  • Clinical Research Coordination/Management
  • Regulatory Affairs/Operations
  • Business
  • Trial Records Management
  • Clinical Process
  • Clinical Trial Compliance
  • Clinical Development
  • Quality Assurance/Control/ Operations
  • R&D Quality Management
  • Strategic Operations and Planning
  • Global Development
  • R&D IS Management
  • Archives

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