The University of Florida (UF) is committed to protecting the rights and welfare of participants involved in human research. This institutional mission is led by UF’s Human Research Protection Program (HRPP) which provides oversight, administrative support and educational training to ensure that UF complies with all applicable federal, state, and local regulations / requirements.
UF’s HRPP is not a specific office, rather it consists of multiple components and is lead by the Office of Research. The primary components of the HRPP are:
UF is committed to protecting research participants, upholding ethical standards, and improving our practice at every step. Individuals conducting, supporting or reviewing human research studies should familiarize themselves with all applicable policies. In order to protect participants and stay compliant, all individuals involved in human research should regularly review policies, procedures and guidelines since they are constantly evolving.
This section provides important links to Investigators and Research Staff in order to assist with maintaining compliance with policies, procedures and regulations.
This section is designed to assist former, current, or prospective human research participants in obtaining information or offering input regarding research and clinical trials. It provides important contact information for questions and concerns about participation in research as well as a printable brochure.
In order to demonstrate our commitment to the highest standards in human research participant protections, the University of Florida has applied for accreditation of our Human Research Protection Program (HRPP), including the University’s 3 Institutional Review Boards (IRBs). The accrediting agency is the Association for the Accreditation of Human Research Protection Programs, Inc. (AAHRPP)
AAHRPP is a nonprofit association, founded in 2001, that offers accreditation to institutions engaged in human research. AAHRPP seeks to ensure regulatory compliance, promote practices and identify quality protection programs. AAHRPP’s mission is to work “to protect the rights and welfare of research participants and promote scientifically meritorious and ethically sound research by fostering and advancing the ethical and professional conduct of persons and organizations that engage in research with human participants. AAHRPP achieves its mission by using an accreditation process based on self-assessment, peer review, and education.
The AAHRPP website contains a number of useful documents such as information on AAHRPP’s history and formation, its approach to evaluation, and standards for accrediting human research protection programs.
AAHRPP has designed an accreditation process to help organizations consistently meet ethical principles and standards for protecting research participants. The accreditation process includes two major phases: preparation of a written application addressing each of the AAHRPP accreditation standards and a site visit by a team of professionals assembled by AAHRPP to inspect program operations.
While preparing its written application, the Office of Research conducted a lengthy self-assessment of its operations, including the operations of the UF IRBs, to assure that they complied with AAHRPP’s accreditation standards, federal regulations and federal guidance applicable to human research protections. As a result of this review, the Office of Research as created a new HRPP webpage that includes institutional policies related to our human research protection program. Additionally, all 3 UF IRBs now have one cohesive set of polices, regulatory guidances and Investigator guidelines.
The written application to AAHRPP was approved in September 2017. The second phase of AAHRPP accreditation, the site visit, is scheduled for January 10-12, 2018, and will coordinated by the Office of Research. Within 30 days of the site visit, AAHRPP will provide the University with a written evaluation of its findings. We will then have 30 days to respond to these written comments. The written application, site visit findings, and response to the AAHRPP report are then reviewed by AAHRPP’s Council on Accreditation. The Council then determines whether the institution is granted one of the following statuses: full accreditation, qualified accreditation, accreditation withheld, or accreditation-pending. Full or qualified accreditation is granted for 3 years.
It is important to remember that the protection of human subjects is a SHARED responsibility and we are pursuing accreditation Together! The Office of Research has developed a new Human Research Protection Program (HRPP) website that provides important information about our program, including new institutional HRPP Policies. In addition, the UF IRBS have drafted a series of Investigator Guidelines that compliments their recently revised polices and regulatory guidances, to better assist the UF research community in the protection of human subjects.
Please refer to the UF HRPP web page at http://research.ufl.edu/hrpp.html for more information.
To learn more about AAHRPP, please visit http://www.aahrpp.org/
If you have any questions regarding UF’s HRPP and/or AAHRPP accreditation, please contact Gailine McCaslin in the Office of Research at (352) 273-3407 or firstname.lastname@example.org.
As one of the leading public research institution in the nation, the University of Florida is committed to excellence in human subject protection. AAHRPP accreditation will not only validated how well we share the responsibility of protecting the rights and welfare of human research participants, but also demonstrates our desire to hold ourselves to a higher set of standards than required by federal and state law. Additionally, it is important to note that not only has UF’s Vice President for Research mandated the institution’s pursuit of this accreditation, but accreditation is also an obligation for State Cancer Center of Excellence Funding.
The site visit team will meet with senior leadership and key members of the HRPP to ask some organizational-based questions and conduct a record review. They then conduct interviews IRB chairs, IRB members, staff, and chairs, as well as investigators and research study team members. They also interview key institutional officials, such as those who review contracts, manage financial conflicts of interest, lead departments involved in research, and provide legal advice.
The AAHRPP team will select people to be interviewed from the HRPP Personnel list provided during the accreditation application process Investigators will be selected who reflect the ranges of experience, protocol volume, types of ongoing research, and research risk levels at the organization. In addition to investigators, site visitors will interview coordinators, co-investigators, and other study team members.
If selected, we will provide you with additional prep reparation to promote a successful interview.
AAHARP is interested in your awareness of and knowledge about key concepts and policies, including, but not limited to:
NOTE: The specific questions you will be asked by the AAHRPP site visitors depends upon your role within the UF HRPP.