30 Minute Webinar: Overview of Mentor IRB

New Sessions Coming in 2020!

During this brief overview we will:

  • show how Mentor IRB can make your team more efficient.
  • address how Mentor Logic makes the protocol submission process easier and faster,
  • discuss how workflow routing reduces your turnaround times and
  • show how our extensive configuration program makes implementation easier for your stakeholders.
  • answer your questions and discuss our simple pricing program.

If you would like a more extensive demonstration of Mentor IRB just let us know!

Coming Soon!

Use and Abuse of IRB

Recorded Session - Link Below

IRBs are prone to mission creep and mis-interpretation of the federal regulations. This webinar focuses on IRB practices in reviewing social science types of research projects. This webinar will guide participants through the application of the regulatory definitions of research and human subjects and minimal risk, the exemption categories, as well as discuss issues of scientific design in relation to risks and benefits. The webinar will also discuss informed consent and the conditions for waiver of informed consent. Our goal is to establish clear boundaries for IRB authority and explore reasons why IRBs often exceed them.

Learning Objectives:

  • Apply the regulatory language that determines if IRB review is required, and if so, at what level.
  • Apply an understanding of the role scientific design plays in review of minimal risk research.
Go To Recorded Session

Evaluating IRB Software Vendors

Recorded Session - Link Below

Join us as we discuss:

  • 4 key criteria for evaluating online IRB systems
  • What to focus on when considering key stakeholders
  • What to ask in the exhibit hall and what to save for follow up
  • 3 sure signs that you are talking to the wrong vendor

Plus, we’ll discuss some easy homework you can do before visiting the exhibit area of a conference.

Go To Recorded Session