Are you utilizing best practices when completing regulatory documents?

Tufts Medical Center and Tufts CTSI Professional Education invite you to join us on September 15 for the next Clinical Research Staff Quarterly Training session. This interactive, live session will highlight best practices for completing and managing regulatory documents for industry-funded clinical trials. We will focus on the regulatory documents that are required before study initiation. You will also learn strategies for keeping a well-organized digital regulatory binder. Plus – participate in a team-based scavenger hunt activity for a chance to win a $5 Dunkin gift card for all team members.

Who Should Attend?

All clinical research staff involved in study start-up for industry-funded trials at Tufts MC are invited.

Featured Speaker

Vidya Iyer, MBBS, CPI, Director of Clinical Research at Tufts Medical Center

Learning Objectives

By the end of this workshop, participants will be able to:

  • Identify the required documents for study start up
  • Distinguish between FDA-required and sponsor-specific forms
  • Discuss tips and tricks for completing regulatory documents
  • Utilize best practices for organizing regulatory forms in digital format (“Regulatory Binder”)


Thursday, September 15, 2022
Live online (a link will be sent to those who register).


To attend, please enroll here via Tufts CTSI I LEARN by noon on September 15, 2022.

For questions and further information, please email Shane Cox.