21th - 23th January, 2020 (Orlando, FL)

 9th Trial Master File Summit

This three-day Summit in the Sunshine State offers attendees premier networking opportunities, access to the TMF community, and endless amounts of educational information to bring back to their teams.

Since the TMF community has enjoyed the event based on education, collaboration, and networking, creating a plethora of resources for the industry and this year’s Summit will expand upon that legacy. Focusing on six key areas, the 9th Trial Master File Summit will arm attendees with actionable strategies and useful tools to bring back to their organization.

The 9th Trial Master File Summit features:
• An education-driven program, guided by your peer’s evaluations, copious amounts of research and conversations with our esteemed advisory board
• Three days, three hands-on courses and six tracks to tailor each attendees experience
• Detailed case studies and information sessions featuring lessons learned in TMF operations, partnerships, functional areas, Quality, inspection readiness, and eTMF/technology enhancements
• More than 45 expert speakers from diverse backgrounds in clinical document management
• 10 hours of networking with the TMF community

Summit participants return to work informed, equipped, and inspired to guide their organization’s TMF to its full potential! Focuses and new features of this year’s program include: Four workshops for varying experience-levels, Inspection experience showcase, Functional area collaboration, TMF operations, Quality and completeness, eTMF/technology enhancements, Partnerships, Inspection readiness.

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

For more details: http://bit.ly/2muJVXS

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