Investigator Resources

ICTR Resources

The UMB ICTR provides financial support as well as infrastructure, environment, training, and workforce to invigorate, facilitate, and accelerate clinical translational research to improve patient and community health.

GCRC Resources

• Nursing Resources  
• Research Subject Advocate

GCRC Application

• Application Process 

Education and Training

• UMB Programs 
• External Training Links

GCRC Forms

• GCRC Patient Registration Form
• Adverse Event 
• Protocol Deviation Form

Useful Research Links

University of Maryland Resources

• Human Research Protections Office (HRPO)  
• Center for Clinical Trials  
• Environmental Health and Safety  
• Office of Research  
• Office of Research Development  
• Baltimore VA Medical Center  
• School of Medicine Mentoring Program    

Federal Agencies

• Office of Human Research Protection (OHRP)  
• Food and Drug Administration (FDA)  
• Office of Research Integrity (ORI)  
• National Institutes for Health (NIH)  
• Veterans Administration (VA)    

Good Clinical Practice

• Good Clinical Practice in FDA-Regulated Clinical Trials  

Other Resources

• RegSource (Free portal organizing worldwide Regulatory, Clinical, Toxicological, CMC and other drug/device development-related information on the Internet)
• ClinicalTrials.gov  
• Certificates of Confidentiality  
• Bioethics Resources  
• The Hastings Center  
• Public Responsibility in Medicine and Research (PRIM&R)  
• Agency for Healthcare Research and Quality (AHRQ)  
• Common Terminology Criteria for Adverse Events v3.0 (CTCAE)