June 9-10, 2022
Online Livestream
2nd Risk Based Quality ManagementSummit
World Class Risk Evaluation and Data Monitoring
Days
Hours
Minutes
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The clinical trial landscape has shifted as a result of COVID-19 and quality risk management techniques and tools have ensued by leaps and bounds over the last year. Best practices in RBQM are influencing clinical study methodology and decentralized trials, putting a spotlight on risk based data review including site and central monitoring.
One of the challenges of harnessing RBQM to its fullest potential lies in the opportunity to remove silos and work toward more integrated solutions and processes. DGE invites you to attend the 2nd Annual RBQM Summit and hear from industry experts about the details of implementing data flow process maps, audit trails, data monitoring tools and a deep dive into quality tolerance limits.
Agenda at a Glance
Topics covered will include:
  • Cultivate a “culture of quality” and ensure end-to-end RBQM
  • Expand monitoring to include remote data monitoring, site and central monitoring
  • Sharpen skills for risk identification, mitigation and response
  • Consider why QTLs and KRIs must line up and how QTL management can be more robust
  • Engage sites to respond to central monitoring outputs
Top Reasons to Attend
  • Gain a timely update from industry experts on new tools and techniques for managing RBQM
  • Take a deep dive into approaches for advancing remote data, site and centralized monitoring
  • Set reasonable quality tolerance limits and improve your method for QTL management
  • Reshape how your study gets audited
  • Determine what data is trending and how best to utilize it toward an adaptive approach to risk management
Who Should Attend
  • RBM/RBQM
  • Study Monitoring
  • Study Monitoring
  • Clinical Operations
  • Clinical Research
  • Clinical Quality
  • Clinical Quality Assurance
  • Clinical Compliance
  • Clinical Outsourcing
  • Data Management
  • Data Science
  • Global Clinical Trial Operations
  • Regulatory Affairs
  • Risk Evaluation
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Event Partners
15
Speakers
21
Days
251
Participants
125
Workshops
90
Venue
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