Good Clinical Practice Series

This series will provide guidance from the regulations and practical experience from experienced investigators and coordinators in how to accomplish the best in clinical research management practices.

(Note:Introductory GCP training is available online free for all UT research personnel through the CITI training website. CITI training certification is mandatory to conduct research at UTHSC-Houston.)

Objectives
Enhance GCP training for investigators and clinical research personnel
Enhancing the quality of interaction with CPHS and those affiliated with clinical trials.
Discussing strategies for improving compliance in clinical research practice

*Audience:*	Clinical research investigators, research nurses, coordinators, clinical research administrative and support staff.
Duration:	90 minutes
Location/Time:	MSB 2.135 11:30am to 1:00pm, 2nd Tuesday
No need to register. Lunch will be available for the first 25 participants.
2010 - 2011 Sessions: Oct 11, 2011 - Regulatory Binder Dec 13, 2011 - IND/IDE Regulations Feb 14, 2012 - Data Safety Monitoring Plans Apr 10, 2012 - Quality Management Jun 12, 2012 - Multi-center Trials – Project Management Aug 14, 2012 - Regulatory Inspections For other questions, please call us at 713-500-7910 or email clinicaltrials@uth.tmc.edu