Services & Key Personnel
OUR MISSION
To provide a single portal of resources, expertise, and best practices for investigators
and research staff to facilitate efficient, compliant and ethical study conduct and management.
OUR GOALS
processes and development of clinical trial management tools.
SERVICES PROVIDED
Just give us a call or send us an email to make an appointment - thanks to continued support from CTSA, we are happily able to provide assistance with any and all of the following:
- Protocol development
- Consent form development
- Submission to UT-IRB (CPHS)
- Submission to Chesapeake IRB
- Other IRB Reciprocity
- IND/IDE submission to FDA
- Other submissions to FDA
- Clinicaltrials.gov registration
- Data Safety Monitoring Plan Development (DSMP)
- Formation of Data Safety Monitoring Board (DSMB)
- Budgeting and Billing
KEY PERSONNEL
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Sujatha Sridhar, MBBS, MCE |
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Ngozi Okafor |
Thea Troetscher, RN |
Marilyn Perry, CCRP |
Catrina Coverdale, CCRC |
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University Center Tower We are located at the corner of Pressler and Fannin |
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Email us directly, or send suggestions, comments through . . .
IQ BOX
Do you have an idea to improve the clinical research review and conduct UTHealth?
Do you just want to vent about something affecting your work?
Or, do you have a question regarding GCP, IRB, iRIS or clinical research management?
Let us know via the IQ Box!
OFFICE OF RESEARCH | CLINICAL TRIALS RESOURCE CENTER |
COMMITTEE FOR THE PROTECTION OF HUMAN SUBJECTS |ANIMAL RESEARCH | ENVIRONMENTAL HEALTH & SAFETY | CORE LABORATORIES | SPONSORED PROJECTS | TECHNOLOGY MANAGEMENT
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Clinical Trials Resource Center (CTRC) last modified March 21, 2013 |
