EpiNet - Web-based Patient Registry Software for Clinicians and Researchers

• Dashboard view for quick overview of a Clinician’s assigned patients
• Detailed patient summary
• Multiple sophisticated data collection forms
• Data entry approval system with levels of accreditation
• Multiple registries for handling different patient sets
• Automated scheduled follow up reminders
• Condition comparison charting
• Data extract
• Reporting on key data
• Encourages optimal management of the patient
• Provides a central repository, accessible worldwide
• Created in partnership with the Auckland District Health Board

A registry for capturing data on patient episodes triggered by a medical condition; enables tracking and monitoring of outcomes based on approved treatments provided.

• Improve clinical care of patients
• Dynamic clinical support, designed to capture relevant clinical data only
• Control access and entry of data by role:
  • Read-only access
  • Research Assistant – requires approval from investigator
  • Investigator
  • Primary Investigator (owner) for a specific patient
  • Anonymised administrator access
• The investigator who enters the information (the primary investigator) determines who can access the record
• Low-cost, collaborative approach to research
• Accessible from anywhere in the world
• Information on patients with specific syndromes allowing for focused studies
• Identification of relatively large groups of patients with uncommon or rare syndromes, so that research in these patient groups can be facilitated
• Data collection tool, not intended for use as a clinical trial