Designed to Produce

Study Start-Up Services

Your Stiris team is dedicated to rapid site activation. Our specialists review each study and individualize the start-up process to address your protocol’s specific needs to ensure the most efficient and effective structure for your study.

Stiris’ start-up services include:

  • Site identification
  • Feasibility
  • Regulatory Affairs support
  • Ethics submission
  • Essential document dissemination, collection, review and tracking
  • Investigator contract closing
  • Trial Master File set-up

We emphasize developing a solid plan from the beginning, produced in cooperation with your clinical team.

Because clear, well thought out direction, with a common vision ensures effective start-up and long term management of your clinical trial.