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Improve RBM Process and System Interoperability to Optimize Data Quality and Trial Efficiency

November 2-3, 2017
  • Philadelphia, PA

CBI’s Risk-Based Trial Management and Monitoring conference is dedicated to reducing the complexity of implementing an efficient RBM methodology and providing real-world strategies to system adoption and process integration.

The concept of RBM is nothing new, however many questions still remain: Are we making it more complex than it needs to be? How can we work more effectively with sites and other stakeholders? How can we demystify and implement complex RBM models in a straightforward manner? And now, with each organization collecting clinical data across multiple systems, usually in their own format and reporting environments, the integration of data has become increasingly difficult.

Join your peers, RBM thought-leaders and trial counterparts in November to collaborate on the growing challenges and solutions for ensuring RBM data quality, maximizing the efficiency of your trials and adhering to regulatory expectations.

What’s New in 2017?

  • Examine the ICH E6 guidelines and how it is expected to affect industry
  • Gain critical insights into regulatory expectations of RBM trials vs. other clinical trials
  • Utilize mobile technology to ease the burden on sites and patients
  • Hear successes and lessons learned through industry leading case studies on different clinical studies and programs who have made it through an FDA submission
  • Develop robust change management strategies to promote sustainable RBM implementation tactics
  • Leverage the eSource tool to facilitate RBM
  • Learn the site perspective on the integrating RBM into site processes and how it has aided in overcoming complex monitoring challenges

Previous Attendee Acclaim:

My company is just starting to implement RBM. This conference helped me understand A-Z all the details that will be needed – exciting!

Senior CRA, Regeneron

The ideal forum to be on the forefront of emerging strategies and approaches to clinical trial oversight.

Manager, Clinical Monitoring, St. Jude Medical

Great conference – nice broad array of attendees from different side of the business – gives good perspective.

Information Strategist, Pfizer

This conference was a great way to get the pulse of RBM across the industry and prepare for the next steps as it evolves.

Associate Director, Clinical Innovation, INC Research

November 2-3, 2017 | Philadelphia, PA

Risk-Based Trial Management and Monitoring 2017

Improve RBM Process and System Interoperability to Optimize Data Quality and Trial Efficiency

CBI’s Risk-Based Trial Management and Monitoring conference is dedicated to reducing the complexity of implementing an efficient RBM methodology and providing real-world strategies to system adoption and process integration.

The concept of RBM is nothing new, however many questions still remain: Are we making it more complex than it needs to be? How can we work more effectively with sites and other stakeholders? How can we demystify and implement complex RBM models in a straightforward manner? And now, with each organization collecting clinical data across multiple systems, usually in their own format and reporting environments, the integration of data has become increasingly difficult.

Join your peers, RBM thought-leaders and trial counterparts in November to collaborate on the growing challenges and solutions for ensuring RBM data quality, maximizing the efficiency of your trials and adhering to regulatory expectations.

What’s New in 2017?

  • Examine the ICH E6 guidelines and how it is expected to affect industry
  • Gain critical insights into regulatory expectations of RBM trials vs. other clinical trials
  • Utilize mobile technology to ease the burden on sites and patients
  • Hear successes and lessons learned through industry leading case studies on different clinical studies and programs who have made it through an FDA submission
  • Develop robust change management strategies to promote sustainable RBM implementation tactics
  • Leverage the eSource tool to facilitate RBM
  • Learn the site perspective on the integrating RBM into site processes and how it has aided in overcoming complex monitoring challenges

Previous Attendee Acclaim:

My company is just starting to implement RBM. This conference helped me understand A-Z all the details that will be needed – exciting!

Senior CRA, Regeneron

The ideal forum to be on the forefront of emerging strategies and approaches to clinical trial oversight.

Manager, Clinical Monitoring, St. Jude Medical

Great conference – nice broad array of attendees from different side of the business – gives good perspective.

Information Strategist, Pfizer

This conference was a great way to get the pulse of RBM across the industry and prepare for the next steps as it evolves.

Associate Director, Clinical Innovation, INC Research

November 2-3, 2017 | Philadelphia, PA