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Office of Compliance

Human Research Protection Program (HRPP)

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Conflict of Interest Reporting for Fiscal Year 2010 will begin on July 1, 2009 and is due by September 18, 2009 Click here for more information

NEW FDA GUIDANCE ON REPORTING ADVERSE EVENTS
On January 15, the US Food and Drug Administration posted final guidance for investigators, sponsors, and institutional review boards related to the requirements for reporting adverse events in clinical trials. The new guidance specifies the types of adverse events that should be reported to IRBs who are reviewing events in a multi-center study. Click here for the FDA guidance.


KUMC's Human Research Protection Program Achieves Accreditation
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OHRP Frequently Asked Questions and Answers on Prisoner Research

New OHRP Guidance - January 15, 2007

Accreditation


Research Integrity

FDA Guidance on Investigational Devices



Compliance Helpline


To confidentially report noncompliant conduct:
913-588-5757 or
Toll Free: 877-588-5757
Click here for more information.


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Welcome

The KUMC Human Research Protection Program (HRPP) was developed to ensure the rights, safety and welfare of all subjects recruited or enrolled in research projects, regardless of funding source. The program also ensures that all personnel involved in research activities understand and comply with the ethical standards of research. The HRPP coordinates oversight by incorporating all aspects of compliance related to human subjects research. The components of the HRPP are:


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Consultation and Pre-Review Services

The Human Research Protection Program is pleased to offer Consultation Appointments, to assist investigators, coordinators, residents, and students with pre-review and other questions about HSC submissions. Half-hour appointments will be offered during the following times:

Mondays: 11 a.m. - 1 p.m.
Wednesdays: 11 a.m. - 1 p.m.
Fridays: 2 p.m. - 3 p.m.


Other times can be arranged when requested. Investigators may use the 30-minute time slot for help in evaluating the feasibility of a project and possible regulatory implications, pre-review of your draft HSC application, protocol and consent form, assistance with answering provisos, and general questions about HSC and other regulatory requirements. To schedule an appointment, please contact the HRPP Director at 588-0942 or the HSC Office at 588-1240.


KUMC's Human Research Protection Program Achieves Accreditation

WASHINGTON, DC, Sept. 19, 2007 -- The Association for the Accreditation of Human Research Protection Programs, Inc. (AAHRPP) today announced the first organizations to be accredited in the states of Kansas, Oklahoma and West Virginia, and the Commonwealth of Puerto Rico. The list includes both major universities and nine Veterans Affairs facilities and now brings the number of states with AAHRPP-accredited organizations to 32 (including the Commonwealth of Puerto Rico). The following were received full accreditation
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