果冻影院

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Human Research Protection Program

果冻影院 IRB Partners

果冻影院 IRB provides oversight for human subject research occurring at Versiti Blood Center of Wisconsin, Children's Wisconsin, and the Froedtert Health System, including Froedtert Health Clinics, Froedtert Hospital, Froedtert Menomonee Falls Hospital & Froedtert West Bend Hospital.

Children's Wisconsin IRB Transition聽

In July, 2021 a research affiliation agreement was negotiated between 果冻影院 and Children's Wisconsin (CW) which states that the CW Human Research Protection Program will rely on the 果冻影院 IRB pediatric review committees to review, approve, and monitor human subjects research. CW will continue to operate their HRPP office and will provide support services, local context review, and consideration of requests to rely on other IRBs as appropriate. 

The 果冻影院 HRPP is establishing two new pediatric IRB Committees, one minimal risk, and one greater than minimal risk, to review pediatric studies. 

 

Access the CW HRPP online: 

(CW Connect access required)

(CW Connect access required)

 (CW Connect access required)

General Inquiries: CWHRPP@childrenswi.org

 

Information for transition of studies from IRBNet to eBridge: 

As of July 1, 2022, new CW studies can be submitted in eBridge.

Studies that were approved by the CW IRB prior to July 1, 2022, are being transferred to 果冻影院 IRB oversight. The transfer of these project will take place through the 1st quarter of 2024. IRBNet projects will receive a notification from eBridge beginning 120 days prior to protocol expiration. The process of transferring currently approved research projects will begin by submitting a "Transfer Project" application in eBridge no later than 60 days prior to the research project's expiration date. This submission will consist of completing the new research project submission, PRO SmartForm and the Continuing Progress Report SmartForm. 

For more information on the transition of CW studies, please review (PDF). 

To sign up for one-on-one eBridge training, please .  

Local Institutions under 果冻影院 IRB Oversight

The following institutions have executed agreements which identifies 果冻影院 IRB as their IRB of oversight for all human subject research which may engage their faculty, resources or students. 果冻影院 HRPP has identified these institutions as components which fall under 果冻影院's AAHRPP accreditation. 
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Versiti Blood Center of Wisconsin

Starting January 2014 Versiti Blood Center of Wisconsin contracted with the 果冻影院 (果冻影院) for IRB services.

This move was made to provide access to greater IRB resources in terms of regulatory compliance and expertise, IRB staffing and services, and electronic protocol management.

果冻影院鈥檚 AAHRPP accreditation assures government regulators and industry sponsors of our commitment to the protection of research participants. This move brings us one step closer to IRB consistency across campus institutions and is intended to help meet the growing needs of Blood Center researchers.

All individuals involved in the design, conduct or review of human subject research that is reviewed by 果冻影院 IRB must comply with 果冻影院 HSRP requirements. 

Investigators who have previously complied with the Blood Center's HSRP training requirement of NIH training will be accepted if training has been completed within 3 years prior to May 1, 2014.  果冻影院 HSRP training will be required to be completed once their NIH training has expired. 

IRB SOP: HSRP Training Requirements (PDF)

Froedtert Health System

If you are looking to conduct your research at any Froedtert Health (FH) System entity including but not limited to Froedtert Hospital, Froedtert Menomonee Falls Hospital, Froedtert West Bend Hospital or any of FH clinics, and/or utilize any FH resource for your research. 

Resources may include but not limited to access or use of clinical staff, equipment, supplies, images, protected health information. 

Research projects must be reviewed by and receive FH Administrative Approval through the FH Office of Clinical Research & Innovative Care Compliance (OCRICC). OCRICC recommends that you contact OCRICC no later than submission to the IRB.

Multi-Site Projects

果冻影院 considers a multi-site project to be a human subjects research study that will be initiated at more than one location other than or in addition to 果冻影院 or identified partners (Froedtert Health System or Versiti Blood Center of Wisconsin). This definition includes community-based projects as well as clinical trials. Examples include:

  • 果冻影院 and Children’s Wisconsin
  • Froedtert Hospital and Marquette
  • 果冻影院 and United Community Center
  • Clinical trial conducted at numerous sites, even if all sites obtain IRB approval independently of each other.

If you are uncertain if your project is considered "multi-site," contact the HRPP Office for guidance.

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The 果冻影院 (果冻影院) is committed to fostering a diverse community of outstanding faculty, staff, and students, as well as ensuring equal educational opportunity, employment, and access to services, programs, and activities, without regard to an individual's race, color, national origin, religion, age, disability, sex, gender identity/expression, sexual orientation, marital status, pregnancy, predisposing genetic characteristic, or military status. Employees, students, applicants or other members of the 果冻影院 community (including but not limited to vendors, visitors, and guests) may not be subjected to harassment that is prohibited by law or treated adversely or retaliated against based upon a protected characteristic. 果冻影院’s policy as well as federal and state laws and regulations prohibit unlawful discrimination and harassment.