The Office of Human Research Protection provides a focus and guiding set of principles to assure patient safety, the provision of full and informed consent by participants, and guidelines for researchers as to the ethical conduct of research and the ensuing scientific publication.
For questions or to learn more about the Office of Human Research Protection, contact:
Lynda J. Dimitroff, PhD, MSEd, BSN, LMHC-LP, RN, MCHES, PCC
Chair, Institutional Review Board
Lynda.Dimitroff@rochesterregional.org
Renee Capizzi, RN, RAC
IRB Administrator
Renee.Capizzi@rochesterregional.org
Lauren Fenclau
IRB Coordinator
Lauren.Fenclau@rochesterregional.org
Resources
Human Research Subject Protection Certifications
- CITI Course Program Course Instructions
- CITI Human Research Subjects Certification Training
- Committee members – take IRB member modules
- Principal and sub investigators – Principal Investigation modules
- Coordinators – research coordinator modules
- Renewals (every 3 years) – refresher course every 3 years modules
- Human Research Subjects Protection Training
Federal Regulations
- Code of Federal Regulations Title 21 Part 312 (FDA IND Regs)
- Code of Federal Regulations Title 21 Part 812 (FDA IDE Regs)
- Code of Federal Regulations Title 21 Part 50 (Protection of Human Subjects)
- Code of Federal Regulations Title 21 Part 56 (Institutional Review Board)
- Belmont Report
- CenterWatch Clinical Trials
- Center for Disease Control
- Medical Dictionary