Pages Tagged: IRB / Human Subjects
Found 19 pages with this tag.
Frequently Asked Questions about Human Subject Research (IRB)
Find answers to frequently asked questions about human research at Syracuse University, including IRB requirements, review processes, and compliance guidance.
Get support for human research at Syracuse University through consultations, guidance, and resources to help navigate IRB requirements and the review process.
Institutional Profile, UEI No., and Compliance Information
Find Syracuse University’s DUNS number, UEI, tax ID, and current F&A, fringe benefit, and compliance rates. Access key institutional data and resources for sponsored program proposals and reporting.
Students as Research Participants
Research with one's own students presents unique considerations with regard to human subjects protections.
Report a Human Subjects Research Concern
Report human subjects research concerns at Syracuse University. Ensure participant safety and ethical compliance through ORIP.
Research Participant Information
Research participants are encouraged to express any concerns or complaints regarding involvement in a research study.
Policies and Guidelines - Human Subject Research
Access key federal regulations, institutional policies, data security standards, and resources that guide human subject research and ensure compliance with ethical and legal requirements.
View submission deadlines and meeting dates for full board IRB reviews at Syracuse University, with details on electronic submission and guidance for expedited and exempt applications.
Find all current Syracuse University Human Research forms, applications, consent templates, guides, and resources to support IRB submissions, study approvals, and compliance with research regulations.
General Data Protection Regulation (GDPR)
Learn how Syracuse University researchers comply with the EU General Data Protection Regulation (GDPR) when handling personal data in research.
Guidance for closing human research studies, including IRB study closure, continuing review, and record retention requirements for compliance.
Guidance for managing human research studies after IRB approval, including continuing review, amendments, reporting, and maintaining compliance.
Preparing a New Study: The Review Process
Learn how to prepare a new human research study, determine IRB review type, protect participants’ privacy, and submit compliant applications.
Explore Syracuse University’s guidance on the Common Rule, federal regulations for protecting human subjects in research studies.
Office of Research Integrity and Protections
Syracuse University’s Office of Research Integrity and Protections supports ethical, compliant research by overseeing human and animal studies, training, and regulatory guidance.
Syracuse University provides guidance and resources to ensure research compliance, ethical conduct and safety in all sponsored projects.
Conducting A Human Research Study
Learn how to conduct human research at Syracuse University, including IRB approval, ethical guidelines, and compliance with federal regulations.
Syracuse University guides researchers in registering and reporting NIH-funded clinical trials on ClinicalTrials.gov, ensuring compliance, ethics, and transparency.
Learn about Syracuse University’s IRB processes, policies, and resources for conducting ethical research involving human participants.