Children's Hospital of Wisconsin logo   spacing image
About Children's Hospital and Health Systemspacing image
Quick Links for:
spacing imageHealth Care Professionalsspacing image
    Search:
                          
Horizontal stripes
spacing imageHomeHealth InformationFind a DoctorMaps & DirectionsGiving & VolunteeringNews & CalendarResearchCommunity ProgramsGift ShopCareersspacing image

  Overview
 
 
Side navigation, highlighted area, top left Side navigation, highlighted area, top center Side navigation, highlighted area, top right
  For Researchers and Staff
spacing image spacing image
spacing image Cores
spacing image spacing image
spacing image General Clinical Research Center
spacing image spacing image
spacing image Human Research Review Board
spacing image spacing image
spacing image Internal Funding
spacing image spacing image
spacing image Policies and Procedures
spacing image spacing image
spacing image Resources
spacing image spacing image
spacing image Advances in Research
 
Side navigation, highlighted area, bottom left Side navigation, highlighted area, bottom center Side navigation, highlighted area, bottom right
 
  Investigators at CRI
 
  Translational Research Programs
 
  Newsletters
 
  Current research at CRI
 
  Newsroom
 
  Events
 
  Support CRI
 
spacing image
spacing image spacing image E-mail this page E-mail this page     Print this page Print this page
spacing image spacing image

IRBNet quick start:

New submissions

  1. Log onto IRBNet at http://www.irbnet.org. If you have not registered for IRBnet, please refer to our IRBNet instructions on the Children's Hospital of Wisconsin HRRB home page. Training for this application is done on an ongoing basis and can be scheduled through the HRRB office.
  2. Download all necessary forms and applicable checklists (you may want to print this out for your reference). Modify the approved templates given to construct your study documents.
  3. Upload your customized study documents into the Study Designer and fill out the Registration Form Wizard as it applies to your study.
  4. Obtain all required signatures prior to submission by sharing your study with appropriate personnel. The "Signature Contact Information" page can be found in the Reference and Forms Library in IRBNet. Obtaining all signatures prior to submission will expedite your approval process.
  5. Double-check your submission for completion and click submit. Once a study has been submitted, it is locked by the board and you will not be able to make edits. To add documents to a previously submitted submission, a new package will be created. Please delete any forms previously submitted or flag additional documentation for the reviewer.
  6. Upon review, you may be required to either upload modifications per the reviewer's request or answer questions regarding your study. Please respond promptly in order to facilitate a quick approval. Once your study has been approved, you will find your approval packet online in the Study Designer under "Human Research Review Board Documents."

 

 

FYI/Guidance:

Informed consent elements specific to research involving DNA testing.                                                 

The 2008 edition of the International Compilation of Human Subject Protections is now available online.

For previously approved protocols:

 

Amendment form

Version 10.31.07

Deviation report

Version 03.28.07

On-site serious adverse event report 

Version 04.25.07

Off-site serious adverse event report 

Version 04.25.07

Continuing review form

Version 10.30.07

 

Additional forms:

Case reports

Emergency use protocol

Non-English speaking consent

Consent to photograph 

Research Personnel Form

Preparatory Research Form

Research billing:

Children's Hospital of Wisconsin clinical lab list

Letter to patients

Miscellaneous:

Translation service list

Levels of risk (children/adults)

Consenting minor parents

FWA information

Links to CITI and Ethics Training

spacing image Arrow Back to top
spacing image page footer spacing image
spacing image
spacing image