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 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

 

  
 Past Participants of the TMF Summit Include

AbbVie

Agios Pharmaceuticals

Alexion Pharmaceuticals

Amgen

AstraZeneca

Bayer

Biogen

Boehringer Ingleheim

Chiesi

Chugai Pharmaceutical

Daiichi Sankyo

Eli Lilly and Company

Gilead Sciences

GSK

Merck

Novartis

Novo Nordisk

Ono Pharma

Orion Pharma

Pharmacyclics

PRA Health Sciences

PSI CRO

Sanofi

Worldwide Clinical Trials