Trifecta’s Clinical Site Management Solutions

By centralizing information and automating administrative processes, our software solutions can improve workflow and save study teams significant time.

SiteReady®: A workflow system that reduces site start-up time for clinical trials


SiteReady® is a fully automated workflow system for the distribution, tracking and collection of study start-up documents that simplifies the cumbersome process for sites, sponsors and CROs.

SiteReady® accelerates the completion of the regulatory document exchange process, eliminating paperwork, FedEx® expense and the tedious back-and-forth of communications and corrections. The result? Reduced start-up timelines and explicit control over the document management process.

Here’s what SiteReady® does for you:

  • Centralizes and displays the current document status for all sites
  • Provides total document version control, efficiently tracking updates and corrections
  • Alerts sites to any actions required and completion status
  • Generates an audit trail tied to each document and action
  • Integrates easily with other site start-up processes to expedite site readiness

Trifecta clients have found that SiteReady® provides critical advantages that traditional trial management solutions simply do not — more document accuracy, document control and exchange, control over compliancy, and less administrative burden.

Interested in getting sites up and running faster?

Let’s talk about ways to make processes more efficient and gain enrollment time.

Contact Trifecta