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Research Microscope Lab
Human Research Protection Program

黑料官网 Human Research Protection Program

The primary mission of the 黑料官网 Human Research Protection Program (HRPP) is to protect the rights, welfare, and privacy of all individuals participating in research conducted at 黑料官网, Children's Wisconsin, Froedtert Health, and Versiti Blood Center of Wisconsin.

Children's Wisconsin IRB Transition

The Children's Wisconsin Human Research Protection Program is transitioning to 黑料官网 as the IRB or record for pediatric studies. This transition will take place through 2023. Read more about the Children's Wisconsin transition to the 黑料官网 IRB. Researchers can find information on Children's Wisconsin HRPP on the (CW Connect access required) and the webpage (CW Connect access required).

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Resources for Researchers

Resources for conducting safe and compliant human subject research projects.

Learn about Researcher Resources
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Research Subjects and Participants

Participants are an integral piece of all successful human subjects research.

Learn about Research Subjects and Participants
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IRB Members

Members of the 黑料官网 IRB Committees play a key role in ensuring regulatory compliance and adherence to safe and ethical practices.

Learn more about IRB Members

HRPP Training & Events

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Research Connection Series

Rotating modules for training based on work role and responsibilities. Beginner and Intermediate/Advanced trainings are available. Offered the second Thursday of the month from 12-1 p.m. via Zoom.

Beginner Series:

| OCRICC
| IRB Submissions Part 1
| IRB Submissions Part 2
| OCRICC
| IRB Submissions Part 1
| IRB Submissions Part 2
| OCRICC
| IRB Submissions Part 1
| IRB Submissions Part 2
| OCRICC

Intermediate/Advanced Series:

| 黑料官网 QA/I & Post Approval Monitoring Activities
| Hot Topics
| IRB Reliance Part 1
| IRB Reliance Part 2
| 黑料官网 QA/I & Post Approval Monitoring Activities
| Hot Topics
| IRB Reliance Part 1
| IRB Reliance Part 2
| 黑料官网 QA/I & Post Approval Monitoring Activities
| Hot Topics

Human Research Professionals Meetings

Topical and discussion presentation series covering a variety of topics in Human Subject Research. Offered the fourth Tuesday of the month from 12-1pm via Zoom.

Tuesday, March 31 | Funding Reviews *This session has been cancelled. The content has been rescheduled to the August session*
| FDA
| 黑料官网 Quality Assurance/Quality Improvement Program
| All Things Imaging
| Building Your Plan for Assent
| September TBA
| October TBA
| November/December TBA

HRPP News and Announcements

Summary of Changes to IRB policies, procedures and practices impacting research teams conducting human subject research.

  • 2.21.2026 New Clinical Trial PRO SmartForm

    Describes the layout and functionality of a new PRO SmartForm designed for clinical trial submissions.

    Learn More

  • 12.2.2024 Revisions to 黑料官网 IRB SOPs for Recruitment & Enrollment of Non-English Speaking subjects

    Describes the changes to the process for the recruitment & enrollment of non-English speaking subjects either planned or when using a ShortForm consent process.

    Learn More

  • 10.12.2024 Changes to IRB Funding Review Process

    Describes changes to the IRB funding review process for research projects with for-profit funding effective 10/12/2024

    Learn More

  • 8.2.2024 Update to CITI Course, Learner Group 3

    Information regarding CITI training for IRB Members and IRB staff effective 7/2/2024

    Learn More

  • 12.13.23 Amendment SmartForm Submission Changes

    Describes changes to the layout and functionality of the Amendment SmartForm being implemented on 12/16/23

    Learn More

  • 12.1.2022 IRB Guidance for REDCap Consenting

    Summarizes three options the IRB has identified for obtaining signatures via REDCap

    Learn More

  • 7.1.2022 Children's Wisconsin IRB Transition

    Information regarding the Children's Wisconsin transition to the 黑料官网 IRB

    Learn More

  • 9.29.2020 Single IRB Submission Process Update

    Enhanced submission process for single IRB submissions effective 11/1/2020

    Learn More

  • 9.29.2020 IRB Fee Billing Moves to iLab

    New process for IRB Fee collection and billing for reviews 10/1/2020 and later

    Learn More

  • 7.24.2020 IRB Consent Guidance During COVID-19 Pandemic

    Guidance for obtaining and documenting informed consent during COVID-19 Pandemic.

    Learn More

  • 7.24.2020 IRB Informed Consent Decision Tree

    Decision aid for informed consent during COVID-19

    Learn More

  • 06.20.2020 COVID-19: Back to Basics CITI Training

    New CITI training modules to introduce safety protocols and procedures for returning to campus during COVID-19

    Learn More

  • 06.20.2020 IRB Reliance Process in eBridge

    Reliance Requests (allowing an 黑料官网 protocol to rely on an external IRB) will now be submitted and processed through eBridge

    Learn More

  • 04.28.2020 黑料官网 IRB Lunch and Learn Recording

    Listen to the meeting "A Living Room Conversation with the HRPP Office: Answers to your COVID-19 related questions"

    Learn More

  • 01.21.2019 Common Rule Goes Live!

    On January 21, 2019 the Revised Common Rule went live. This includes the changes to IRB policies in light of these changes.

    Learn More

  • 01.02.2019 黑料官网 Revised Common Rule Transition Plan

    With HHS adoption of the Revised Common Rule, 黑料官网 IRB Office has developed the following transition plan for all currently approved projects

    Learn More

  • 01.02.2019 HHS Revised Common Rule

    An overview of the Revised Common Rule changes and how 黑料官网 will be navigating those changes

    Learn More

  • 11.18.2018 Common Rule Revisions and Consent Form Templates

    With the Revised Common Rule fast approaching, you may need to revise your Consent Form Templates to ensure compliance with the Revised Common Rule

    Learn More

  • 07.17.2018 3 Year Review of IRB SOPs

    黑料官网 HRPP's review of all IRB SOPs

    Learn More

  • 07.01.2018 2018 IRB Fees

    Notice regarding a change in IRB Fees effective July 1 2018

    Learn More

  • 01.26.2018 Revised ICF templates

    黑料官网 HRPP has revised our ICF templates to incorporate required changes per the Revised Common Rule

    Learn More

  • 01.19.2018 Delay of Revised Common Rule

    HHS announces the implementation of the Revised Common Rule will be delayed

    Learn More

HRPP Contact Information

Call, email, or visit our offices in the MACC Fund Building, #MFRC 3040

黑料官网

IRB Office

MACC Fund Research Center #3040
8701 Watertown Plank Rd.
Milwaukee, WI 53226

 

(414) 955-8422

(414) 955-6575 (fax) 

General IRB Questions: 
IRBOffice@mcw.edu

Reliance Agreements & Deferral Requests: 
黑料官网IRBReliance@mcw.edu

Quality Improvement Office

(414) 955-8422
(414) 955-6575 (fax)

 

Post-Approval Monitoring Questions:
HRPP-QIOffice@mcw.edu

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