Main Content

Human Research Office Resources

For Researchers

• Is it human research?
• Developing a protocol
• Investigator responsibilities
• Recruitment and retention
• Registering and reporting results of clinical trials
• External Investigator Research Requests
• The Belmont Report - Ethical Principles and Guidelines for the Protection of Human Subjects of Research - External
• Office for Human Research Protections (OHRP) - External
• AHRQ Informed Consent Toolkit for Minimal Risk Research - External

For Research Participants

• How to Participate in Clinical Trials and Research
• Anatomical gifting to medical science
• About Research Participation - External 
• Clinicaltrials.gov - External
• Office for Human Research Protections (OHRP) - External
• Food and Drug Administration (FDA) - External
• World Health Organization (WHO) - Ensuring ethical standards and procedures for research with human beings - External

UMMC Research Offices

• Office of Research and Sponsored Programs - Pre-Award
• Office of Clinical Trials
• Institutional Biosafety Committee
• Intellectual Property and Commercialization Office
• Radiation Safety Office
• Office of Integrity and Compliance 

The University of Mississippi Medical Center Human Research Office compile, and regularly update, templates to aid local researchers in completing all required study-related documents and meeting all regulatory requirements. Those templates are accessible through the Human Research Office "Resources" page located on the institutional intranet site.