Going from paper to electronic - How to document studies electronically

Presented by Kelly McCormick, MBA, MSL, Regulatory Services Manager, Vanessa Grams, MS, Clinical Research Associate (Monitor), and Kirsten Collins, MS, Clinical Research Associate (Monitor), Clinical and Translational Science Institute.

By the end of the presentation, attendees will:

• Understand what Part 11 compliance is and how to follow it.
• Learn best practices for documenting studies in an electronic format.
• Receive tools and resources for Part 11 compliance and for electronic documentation.

This seminar will be broadcast live via Zoom.

This seminar is part of the bi-weekly Clinical Research Professional Development Series.