Clinical Trials Resource Center

Research Ethics

Intended as informal sessions  for interested UTHealth faculty, students and staff. Paula Knudson will facilitate discussions in which participants may explore history, interpretations, sensitization, informed consent, and how ethics factor into CPHS/IRB decision making. 

Please join us.

Audience: Clinical research investigators, research nurses, coordinators, clinical research administrative and support staff. 

Duration:  90 minutes 

Location/Time: MSB 2.106  -   Each 2nd Thursday, Noon - 01:30pm

No need to register. Lunch available for the first 15 participants.

For other questions, email clinicaltrials@uth.tmc.edu.

ADDITIONAL RESOURCES

CLINICAL RESEARCH UNITS (CRU) | BERD | REDCap
COMMITTEE FOR THE PROTECTION OF HUMAN SUBJECTS |ANIMAL RESEARCH | ENVIRONMENTAL HEALTH & SAFETY | CORE LABORATORIES | SPONSORED PROJECTS TECHNOLOGY MANAGEMENT
OFFICE OF RESEARCH 

Center for Clinical and Translational Sciences

Clinical Trials Resource Center (CTRC)
7000 Fannin Street, Suite 795

Houston, Texas 77030
phone 713-500-3622
fax 713-500-0334
clinicaltrials@uth.tmc.edu

last modified October, 2013
Copyright © 2012
How can we improve this site?