Wendy Tate, PhD, GStat

While clinical trial site selection aids in a trial’s success, it’s critical to maximize the study's time, resources, and funds.

The Belmont Report established informed consent parameters in 1976, but there are no federal regulations surrounding electronic consent.

Most training programs are outdated, unengaging, & redundant. Learn how to make a program achieving both regulatory requirements & your goals

How can sponsors leverage their relationship with their sites to ensure more efficient research?

Part 2 of Q&A from the Clinical Trial Feasibility: Ensuring Success for Clinical Sites webinar outlining why it is important for sites to approach research operations as a business.

Q&A from the Clinical Trial Feasibility: Ensuring Success for Clinical Sites webinar outlining why it is important for sites to approach research operations as a business.