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The eTMF Evaluation and Capability Checklist

Avoid complications in your Clinical Trial Operations by being equipped with the questions you should ask eTMF vendors.

eRegulatory and eSource Capabilities

eTMF Capabilities Covered:

  • Site Connectivity and Access
  • Project Management Capabilities
  • Inspection Readiness
  • Document Management Capabilities
  • Alert and Reporting Capabilities
  • Document Editing Capabilities
  • Platform Compliance with FDA Regulations
  • Access and Permission Capabilities
  • Integration Capabilities
  • Implementation and Support

Avoid Complications

ensure you select the best fit platform for your organization

Expand Site Connectivity

assure research sites can integrate with the platform and increase operational efficiency

Maximize ROI

reach organizational goals and claim the full potential of your future eTMF system

Ensuring the capabilities of any new system to meet your needs and requirements is essential to maximizing the benefits of modern technology. However, for critical technology infrastructure impacting clinical trial operations like the eTMF, it is often difficult to know what questions to ask vendors as you make your decision.

Our team wants to equip you with the tools you need to ask the right questions of any eTMF vendor. Download this list of top capabilities to look for when evaluating a solution.

Guarantee your eTMF solution is flexible, easy-to-use, and innovative in its approach to site connectivity to maximize the benefits of an Electronic Trial Master File in your clinical trial.

Ask the right eTMF questions to make an informed decision.