A robust clinical monitoring management system fully integrated with a Clinical Trial Management System (CTMS) is not only an essential tool for regulatory compliance, but also ensures CRAs are able to efficiently track and complete their tasks.

Evolve meets your monitoring needs, and also integrates this functionality with our unique Electronic Data Capture (EDC) capabilities.

Monitoring Features

• Monitoring Trip Reports
• Build site monitoring visit templates, including standard
  tasks and requirements in a clear, checklist-style format
• Centrally manage monitoring reports
• Complete monitor visit checklists; document
  corrective and preventive action (CAPA) items
• Generate and manage an itemized list of all
  post-visit items that require follow-up or resolution
• Note source documentation reviewed
  and queries submitted, while on-site
• Generate and submit trip reports (both
  electronic and printable versions available)
• Supports e-signature for submission and
  approval of electronic trip reports
• EDC Monitoring
• Electronically monitor submitted data from
  sites using Evolve’s proven workflow
• Issue and resolve queries electronically
• Quickly scan which data entry forms require action in multiple, customizable views - by subject, site, visit, etc.
• Clearly designate CRF status during the QA
  sequence, including Under Review, Source
  Document Verification, and Clean/Locked

Learn more about Evolve's CTMS & EDC features »