Who Should Attend

"I have attended a few years now and I notice it gets better each time. I learn something new every year."Clinical Document Management Specialist, CR BARD

"This was my first summit. Not only did it meet my development goals, but also business related goals. There was relevant and current content, including real case studies. 'I didn't expect to take away as many nuggets from both presenters and other attendees. This was very valuable to me."Supervisor, CTAs | eTMF SME, SEATTLE GENETICS

"As a TMF associate, I enjoy attending this conference to learn about industry trends and seeing how our vertex standards compare across other companies."TMF Associate, VERTEX PHARMACEUTICALS

Who Should Attend

This conference is designed for representatives from pharmaceutical, biotech, medical device and clinical research companies 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

This event is also of interest to:

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

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