WEBINAR DETAILS
  • When
  • About
    High-toxicity oncology trials elevate dropout risk and documentation burden. This session outlines how Gabrail Cancer Center protects completion stability through structured retention workflows, early query control, and inspection-ready documentation from activation forward.

    Who Should Attend
    • Sponsor Data Management Leaders
    • Quality and Compliance Executives
    • Pharmacovigilance Teams
    • Clinical Operations Directors
    • Principal Investigators
  • Agenda
    • Attrition Risk in Oncology Populations: Treatment burden increases dropout without disciplined retention systems.
    • Query Aging and Data Drift: Backlog growth delays database lock and erodes sponsor confidence.
    • Safety Escalation Governance: Clear reporting thresholds protect patient safety and regulatory trust.
    • Inspection Readiness from Activation: Documentation architecture must be built early to prevent late-stage exposure.
    • Completion Velocity as Competitive Advantage: Clean closeout accelerates sponsor milestones and repeat study awards.
    • Q & A – Polls – Handouts We will use polls to capture your priorities, answer questions live, and provide a downloadable Data and Retention control resource.
  • Duration
    1 hour
  • Price
    Free
  • Language
    English
  • OPEN TO
    Everyone
  • Dial-in Number
    Please register for this Webinar to view the dial-in info.
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