Collaborating for Compliance Agenda

Research compliance is an institution-wide undertaking. From investigators and research coordinators to institutional review board members and staff to institutional officials—all members of an institution's human research protections program (HRPP) are key to ensuring high quality, ethical clinical trials. This intensive, half-day version of the program will provide participants with the tools they need to be effective members of their HRPP by highlighting best practices and common compliance pitfalls. The course is designed for all members of an institution's HRPP.

After attending this course, you will be able to:

  • Define various aspects of an HRPP and how those aspects interact with each other
  • Understand how the HRPP fits into a comprehensive compliance program
  • Identify benefits of being involved in a larger institutional program
  • Identify common compliance challenges and collaboratively discuss solutions

Download the PDF of this agenda

Agenda*

September 18, 2015
7:30 AM Registration and Coffee Hour
8:30-8:35 AM Welcome and Introduction
8:35-9:15 AM Understanding Your Institution's HRPP and How it Ensures High-Quality, Ethical Research
  Putting it Together: Defining the Pieces that Make Up the HRPP  and Why They Are Important
9:15-9:45 AM Interactions and Challenges: How Does Your Office/Position Interact With Each Part of the HRPP, and What are the Obstacles and Potential Solutions?
9:45-10:00 AM Break
10:00-11:30 AM Interactions and Challenges cont'd
11:30 AM-12:00 PM Wrap Up Discussion
12:00 PM Adjournment

*Please note the agenda is subject to change.