All research conducted or sponsored by Â鶹ֱ²¥ must comply with strict federal regulations governing the safety of subjects and researchers. Faculty and student researchers must have completed training in various aspects of research conduct governing their work. Training is on-line at no cost to Duquesne faculty, students, and staff. Simply go to the website, register, and list your institution as Â鶹ֱ²¥ and you will find a complete course list including: Institutional Review Board (IRB), Institutional Animal Care and Use Committee (IACUC), Biosafety, Conflict of Interest, and Biomedical Responsible Conduct of Research training.
Human Subjects Research
All research conducted or sponsored by Â鶹ֱ²¥ that involves human subjects must be pre-approved by the Institutional Review Board for Protection of Human Subjects.
is an IRB web-based application that facilitates the submission of proposed research protocols, and monitors the ongoing progress of existing protocols.
Animal Use
All research conducted or sponsored by Â鶹ֱ²¥ that involves live vertebrate animals must be approved by the IACUC before research begins.
HIPAA
The Health Insurance Portability and Accountability Act (HIPAA) emphasize the privacy,
security, and confidentiality of protected health information (PHI) including patient
records, whether in oral, written, or electronic format. Should PHI be the source
of research data from a covered entity, the Institutional Review Board (IRB) must
ensure HIPAA compliance such that the subject's PHI remains confidential. In addition,
the covered entities want assurances that the PHI will be used in accordance with
HIPAA standards. Covered entities are defined as health care providers, such as hospitals,
doctors' offices, health departments, and many others who transmit patient health
information electronically. In addition to health care providers, covered entities
can include insurance companies, human resource offices, health care billing companies,
and others.
Please log in to Mentor, and if applicable, complete the HIPAA forms and follow instructions
located on the Info Page tab under Submitting a Protocol. Contact Joan M. Kiel, Ph.D,
CHPS, Chairperson, University Healthcare Compliance, at kiel@duq.edu.
Biosafety & Radiation Safety
All individuals who intend to acquire, transport or engage in research with the Centers
for Disease Control (CDC), U.S. Department of Agriculture (USDA) Select Agents and
CDC Select Agents, as defined by the CDC and USDA are required to inform the Office
of Research before work can begin. Select Agents are certain viruses, bacteria, rickettsia,
fungi and toxins defined by CDC and the USDA. Research in our laboratories must adhere
to the CDC's guidelines in "Biosafety in Microbial and Biomedical Laboratories", 6th
Edition 2020.
All research conducted at Â鶹ֱ²¥ involving recombinant DNA molecules
must be approved by the Institutional Biosafety Committee (IBC) using the Biosafety
Committee registration document. This must be done before the laboratory phase of
the research begins. Questions concerning this procedure should be directed to the
committee chair, Dr.%20Jan%20Janecka.
Biosafety: All individuals who intend to acquire, transport or engage in research
with CDC, USDA Select Agents and CDC Select Agents, as defined by the (CDC) and the (USDA) are required to inform the Office of Research before work can begin. Select
Agents are certain viruses, bacteria, rickettsia, fungi and toxins defined by CDC
and the USDA. Research in our laboratories must adhere to CDC’s guidelines Biosafety
in Microbial and Biomedical Laboratories, 5th Edition 2007.
The USA PATRIOT Act of 2001 and the Bioterrorism Preparedness Act of 2002, requires
under punishment by fine or imprisonment notification, strict handling and security
procedures for possession, transportation or research work with Select Agents.
The University has adopted an Exposure Control Plan for compliance with OSHA's Bloodborne
Pathogens Exposure Control Program standard. The Plan is administered by the Environmental
Health & Safety Department and training for employees at risk is provided by Duquesne’s
Health Services.
Research Policies (RPs)
Please review the following Â鶹ֱ²¥ administrative policies related to research-
- RP-1 - Procedure for Submitting External Grant Proposals
- RP-2 - The Use of Human Subjects in Research
- RP-3- Effort Reporting on Sponsored Grants and Awards
- RP-4- Governmental, Corporate, Foundation and Privately Sponsored Grants and Awards
- RP-5 - Intellectual Property
- RP-6 - Research Integrity
- RP-7 - Conflict of Interest in Sponsored Grants and Awards
- RP-8- Research Agreements and Private Business Use
- RP-9 - Participation in commercial activities
For more information regarding responsible conduct of research and compliance, contact the Office of Research and Innovation staff.