Come and chat with the IRB staff and members about a variety of topics, such as what the IRB looks for in a consent document and insider tips on getting your protocol through the process faster.
Objectives:
Understanding the CPHS review and approval process.
Enhancing the quality of interaction with CPHS.
Discussing strategies for improving timelines for approval.
Audience:
Clinical research investigators, research nurses, coordinators, clinical research administrative and support staff.
Duration:
90 minutes
Location/Time:
MSB 2.135
11:30am- 1:00pm, 2nd Tuesday
No need to register. Lunch available for the first 25 participants.
2011- 2012 Sessions:
Sep 13, 2011 - Human Subjects Protection Program.
Nov 8, 2011 - Strategies for successful IRB submissions.
Jan 10, 2012 - Tips for Developing Great Consent Documents.
Mar 13, 2012 - Reporting events to CPHS.
May 8, 2012 - Recruitment Strategies – what’s acceptable and what’s not.
Jul 10, 2012 - Common Monitoring Findings and how to avoid them.
PHONE: 713-500-3622 
