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Climedo
Integrated eClinical platform for faster patient reach and real-time data insights

What is Climedo?

Climedo offers a comprehensive eClinical platform designed to streamline clinical data collection and management for various healthcare sectors. The platform integrates electronic data capture (EDC), electronic clinical outcome assessment/patient-reported outcomes (eCOA/ePRO), electronic case report forms (eCRF), and electronic consent (eConsent) solutions. It supports non-interventional studies, real-world evidence (RWE) generation, and medical communication initiatives with real-time data insights into study progress.

The web-based system enables paperless data collection, automated reminders, and reusable forms to enhance data quality and patient compliance. It facilitates decentralized study designs and remote monitoring, allowing for device-independent handling across clinical settings. The platform adapts to organizational processes while maintaining security and user-friendliness for researchers, clinicians, and patients.

Features

  • EDC System: Electronic data capture for clinical studies with real-time insights
  • eCOA/ePRO: Electronic clinical outcome assessment and patient-reported outcomes collection
  • eCRF: Electronic case report forms for structured data entry
  • eConsent: Electronic consent management for patient enrollment
  • Dashboards & Visualizations: Real-time data visualization tools for study progress monitoring
  • Automated Reminders: System-generated notifications to enhance patient compliance
  • Reusable Forms: Pre-built templates for efficient study setup
  • Remote Monitoring: Decentralized study support with device-independent access

Use Cases

  • Conducting non-interventional clinical studies
  • Generating real-world evidence for pharmaceutical products
  • Managing patient-reported outcomes in medical device trials
  • Streamlining data collection for clinical research organizations
  • Facilitating electronic consent in hospital-based research
  • Supporting decentralized clinical trial designs
  • Enhancing medical communication with healthcare professionals
  • Improving data quality in academic research institutes

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