Who Should Attend

Who Should Attend

This conference is designed for representatives from pharmaceutical, biotech, medical device companies as well as CROs with responsibilities in the following areas:

  • TMF and eTMF Process
  • Clinical Document/Data Management
  • Clinical Trial Administration
  • Clinical Operations
  • Regulatory Affairs/Operations
  • Trial, Document and Record Management
  • Clinical Document Coordination
  • Clinical Development/Study Management
  • Quality Assurance/Control/Operations
  • Competency Development
  • Strategic Operations and Planning
  • Quality Management
  • Informatics
  • Clinical IT

This conference is also of interest to:

  • eTMF System Service Providers
  • Data/Records Management Vendors
  • Clinical Research Organizations
  • Paper and Electronic Archiving Solution Providers

Request Event Documentation

Get all of the conference event! Get Event Documentation

Request More Info

For more information regarding TMF Europe, please fill out the form. More Info
live chat software