Enhanced Clinical Trials Research Module

What’s New

• The Research module has been redesigned into a centralized workspace for managing clinical trial information.
• New research sections have been added for:
  – Vitals
  – Lab Results
  – Provider Notes
  – Documents
  – Cancer Staging
• Existing sections including History, Tumor Assessment, Adverse Events, and Concomitant Medications remain available.
• Existing clinical information can now be imported directly into the Research module.
• A new Trial Summary feature allows users to:
  – Select records from multiple research sections
  – Add clinical notes
  – Generate consolidated trial reports
• A dedicated Reports section has been introduced for managing generated trial reports.
• Users can:
  – View reports
  – Assign reports
  – Request sign-off
  – Sign off reports
  – Reopen reports
  – Print reports
• Reports now include additional information such as the Created By field.
• Review and sign-off workflows have been enhanced while maintaining activity logs and export functionality.

How It Works 

• Navigate to Patient > Select Patient > Research.

• Review patient research information using the newly expanded research workspace.

• Import existing clinical information into the appropriate research sections, including Vitals, Lab Results, Provider Notes, Documents, and Cancer Staging.

• Select records from one or more research sections and add them to the Trial Summary.

• Add clinical notes and generate a consolidated Trial Summary report.

• Access the Reports section to review previously generated reports.

• Manage research reports by assigning them for review, requesting and completing sign-offs, reopening or printing reports as needed, while maintaining a complete activity history and sign-off audit trail.

Benefits

• Centralizes clinical trial information into a single research workspace.
• Expands available research data by incorporating vitals, laboratory results, provider notes, documents, and cancer staging.
• Reduces duplicate documentation by importing existing clinical records into research.
• Simplifies collaboration through centralized trial documentation.
• Streamlines report generation using Trial Summary.
• Improves traceability through enhanced activity logs and sign-off workflows.
• Saves time by simplifying research documentation, reporting, and record management.