Who Will Benefit

Who Should Participate

The TMF Institute’s professional development is for representatives from pharmaceutical, biotechnology, and medical device organisations as well as CROs with responsibilities in the 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
  • Trial, Document and Records Management
  • Clinical Document Coordination
  • Clinical Trial Compliance
  • Clinical Development/Study Management
  • Quality Assurance/Control/Operations
  • R&D Quality Management
  • Strategic Operations and Planning
  • Global Development
  • R&D IS Management

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