The University of Arizona

Regulations & Resources

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HSPP Contacts

Department email:

*Subscribe to the HSPP listserv

Christine Melton-Lopez, Director 
(520) 626-8630

Courtney OlsonManager, Process Improvement and Education 
(520) 626-9034

Mason Burchfield, IRB Coordinator
(520) 626-0433

Gina Fimbres, IRB Coordinator
(520) 626-0026

Jessica Winters, IRB Coordinator
(520) 626-0256

Alyssa Little, IRB Associate
(520) 626-5859

Jared Pryor, IRB Associate
(520) 626-1744

Jeff Homes, IRB Associate 
(520) 626-7889

Joanna Schrader, IRB Associate 
(520) 626-6282

Street Address
1618 E. Helen Street
Tucson, AZ 85721

Mailing Address
POB 210409
Tucson, AZ 85721


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Code of Federal Regulations (45 CFR 46) Protection of Human Subjects

FDA Regulations Relating to Good Clinical Practice and Clinical Trials

FDA Form 1572 Investigational New Drug Applications (IND's) Forms & Instructions

EU General Data Protection Regulation


  • Declaration of Helsinki is a set of ethical principles regarding human experimentation developed for the medical community by the World Medical Association (WMA). 

  • Belmont Report is one of the leading works concerning ethics and health care research. Its primary purpose is to protect subjects and participants in clinical trials or research studies. 

  • National Institutes of Health (NIH) Office of Science Policy is the primary policy adviser to the NIH Director on matters of significance to the agency, the research community, and the public.

  • International Compilation of Human Research Standards is a listing of over 1,000 laws, regulations, and guidelines on human subjects protections in 131 countries and from many international organizations.