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Research Microscope Lab
Human Research Protection Program

麻豆学生精品版 Human Research Protection Program

The primary mission of the 麻豆学生精品版 Human Research Protection Program (HRPP) is to protect the rights, welfare, and privacy of all individuals participating in research conducted at MCW, 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 麻豆学生精品版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 麻豆学生精品版IRB. Researchers can find information on Children's Wisconsin HRPP on the (CW Connect access required) and the webpage (CW Connect access required).

HRPP Training & Events

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

Intermediate/Advanced Series:

| Reliance Part 2
| 麻豆学生精品版QA/I Team & Post Approval Monitoring
| Consent & Enrollment of Vulnerable Research Participants
| Reliance Part 1
| Reliance Part 2
| 麻豆学生精品版QA/I Team & Post Approval Monitoring
| Consent & Enrollment of Vulnerable Research Participants

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.

| Dissemination of Research Results
| OnCore Clinical Trials & Financials

HRPP News and Announcements

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

  • 12.2.2024 Revisions to 麻豆学生精品版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 麻豆学生精品版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 麻豆学生精品版protocol to rely on an external IRB) will now be submitted and processed through eBridge

    Learn More

  • 04.28.2020 麻豆学生精品版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 麻豆学生精品版Revised Common Rule Transition Plan

    With HHS adoption of the Revised Common Rule, 麻豆学生精品版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 麻豆学生精品版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

    麻豆学生精品版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

    麻豆学生精品版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

麻豆学生精品版

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: 
MCWIRBReliance@mcw.edu

Quality Improvement Office

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

 

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

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