What to expect at the
Global TMF Summit

The Global Trial Master File Summit is the preferred TMF event, renowned for its exceptional content and high-level speaking faculty.

The Global TMF Summit is known for its networking, actionable lessons, dissemination of best practices, and expertise of speakers on industry trends and trajectories.

Top Reasons to Attend

  • Discuss opportunities to transfer information between systems through artificial intelligence and machine learning
  • Learn strategies for maintaining a compliant TMF according to inspection trends and changing global regulations
  • Comply with oversight and monitoring requirements of with ICH E6(R2) using risk-based approaches and methods
  • Join other clinical functions to implement, migrate, acquire, and remediate systems with optimal interoperability
  • Embrace the beauty of integration and learn common pitfalls as the TMF evolves into a management system

 

 Who Attends

This conference attracts SVPs, VPs, Directors, Heads, and Managers from the pharmaceutical, biotechnology, medical device, CROs, and sites whose responsibilities include:

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

  Past Participants of the TMF Summit Include

  • AbbVie
  • Amgen
  • Biogen
  • Chugai Pharmaceutical
  • Gilead Sciences
  • Novartis
  • Orion Pharma
  • PSI CRO
  • Agios Pharmaceuticals
  • AstraZeneca
  • Boehringer Ingleheim
  • Daiichi Sankyo
  • GSK
  • Novo Nordisk
  • Pharmacyclics
  • Sanofi
  • Alexion Pharmaceuticals
  • Bayer
  • Chiesi
  • Eli Lilly and Company
  • Merck
  • Ono Pharma
  • PRA Health Sciences
  • Worldwide Clinical Trials