Investigator Resources

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)