This educational program is designed and conducted by clinical trial experienced reserach professions from within UT Health. The program examines the entire clinical trial process, from planning to trial close-out activities, and provides pratical recommendations for increasing the efficiency of clinical trial conduct at investigative sites. This program combines didactic presentations and interactive group sessions.

Day 1 focuses on financial management and includes presentations on basic financial principles, research contracting, budget development and billing process.

Day 2 includes discussion about human subjects protections, GCP principles, institutional compliance and consent process.

Day 3 includes presentations on study initiation, study conduct, documetation, investigational devices and drugs and reporting requirements.

Objective:	To provide a model of practice in conducting clinical research based on the principles of Good Clinical Practice, thereby focusing on research compliance, protecting the safety and well-being of the research subject and ensuring integrity of the research
Audience:	Invesigators, research nurses, research coordinators.
*****REGISTER*****
Dates and Location:	April 25 - 8 am to 4 pm at IMM Building 1825 Pressler Street, Houston, Texas 77030 April 26 - 27 - 8 am to 4 noon at MHH Conference Center, 6411 Fannin, Houston, TX 77030
Course Fees Please note course fees for UT Health and MHH participants: Day 1 - $50 Day 2, 3 - $100 Day 1, 2, 3 - $150 Course fees for non UT Health/MHH participants: Day 1 is not open to outside participants. Day 2 + 3 - $600 Questions? Please contact: Linda Gilbert, Training Coordinator - CTRC (713) 500-3621 or Linda.N.Gilbert@uth.tmc.edu.