Change in IRB Member Liaison Support
As you may be aware, the Health Sciences IRBs identify personnel to support IRB members with questions about meeting schedules, review processes (including help navigating ARROW), and any other member-related issues. Our current IRB Member Liaisons are:
IRBReview@medicine.wisc.edu or our main phone number 263-2362.
IRB Member Survey
We will be conducting a survey of all IRB Members in Qualtrics to provide the HS IRBs Office and Chairs with feedback. The questions are meant to elicit your thoughts about the IRB Chairs (and their management of meetings), the HS IRBs Office Staff (and their communication with you, as well as the materials they prepare for meetings), educational materials and experiences, and IRB Member experience. Please keep an eye out for an email asking you to take the survey, which will be sent April 30, 2018.
Delayed Implementation of Revised Common Rule
The Department of Health and Human Services (HHS) issued its final proposal for changes to the Federal Policy for the Protection of Human Subjects (what we know as the "Common Rule") on January 18, 2017. Although the effective date of the revised Common Rule was originally January 19, 2018, HHS postponed implementation until at least July 19, 2018 with the possibility of a further 6-month delay. In the meantime, many of the provisions of the revised Common Rule have been incorporated into campus policy as outlined below. Campus leadership adopted these policies because they allow more studies to qualify for quicker review processes.
Changes to Campus Policies
As of February 19, 2018, several changes to campus policy were made to reduce burdens on study teams while ensuring adequate protection of human subjects. Most of these updates only can apply to research that is NOT federally supported, FDA-regulated, or fall under VA purview. These include:
Anticipating the Common Rule Revisions Relating to Informed Consent
The revised Common Rule will require re-organization of consent documents to begin with a concise and focused presentation of the key information that is most likely to assist in understanding the reasons why one might or might not want to participate in the research.
This approach was incorporated into recently revised campus policies. Additionally, these goals align with the ones we had in mind when overhauling our consent form templates last year.
For over a decade, the Health Sciences IRBs have required study teams to create and use an information sheet for most consent documents longer than 5 pages. We will continue this requirement, but with a small change due to the HS IRBs improved informed consent templates. Going forward, consent forms will be considered to meet the new requirements for presentation of key information if they are:
Consent documents longer than 5 pages and not based on current UW-Madison Health Sciences IRBs templates, or those that are longer than 10 pages even if based on current UW-Madison Health Sciences IRBs templates, will be required to include an information summary sheet.
We allow twice the amount of pages for consent forms based on our current templates because when we overhauled them, we arranged them with a concise and focused presentation of key information most likely to assist subjects in understanding based on community feedback, and also emphasized the use of white space on the page. Using “white space” facilitates understanding but also increases the total page count.