Conducting Trials

conducting clinical trials

Get started here finding helpful forms and guidelines for all your research needs.

Protocol Development - What should be in your protocol? Go here to find templates, outlines and guidelines.

Consent Development - What elements have to be covered? What is the latest required UT-IRB language?

Budgeting & Billing - For what expenses should you plan? What will be required from the Office of Sponsored Projects?

Research Participant Payment (1099) Guidelines - When should you collect W-9 information from participants who are being paid for participation in research?

Recruitment Strategies - Now that you've developed your protocol and consent, how do you plan to get subjects?

Data and Safety Monitoring -When do you need a Data Safety Monitoring Plan? A Data Safety Monitoring Board? Who forms the board?

Quality Management - What are GCP Guidelines for conducting a quality clinical trial?

Study Management - The day-to-day study coordinator experience from pre-study initiation to subject management and drug accountability -get your tips and template forms here.

Lab Certificates - If you will be working with a local lab during the course of clinical trial, then you may need to keep current CAP and CLIA certificates in your regulatory binder. If you need a copy of MHH lab certificates, please, contact the MHH CIRI Research Specialist that is assigned to your trial.

ADDITIONAL RESOURCES

Clinical Trials Resource Center (CTRC)
7000 Fannin Street, Suite 795
Houston, Texas 77030
phone 713-500-3622
fax 713-500-0334
[email protected]