Download: The eTMF Evaluation and Capability Checklist

Avoid complications and headaches when implementing an Electronic Trial Master File solution in your Clinical Trial Operations by being equipped with the questions you should ask vendors.

Ensuring the capabilities of any new system meet your needs and requirements is essential to maximizing the benefits of a new 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.

Download Checklist

Ensuring your eTMF solution is flexible, easy-to-use, and innovative in it’s approach to site connectivity is vital to maximizing the benefits of this technology for your clinical trial.

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

eRegulatory and eSource Capabilities