November 2, 2012
Reportable events and deviations should now be submitted as a New Information submission in eRA.
October 19, 2012
The IRB has modified the Initial Application eForm. The form name has been changed to HRP-211: FORM - Initial Application. It is only accessible within an Initial Application submission in eRA.. If you have any questions please contact the IRB Office.
October 10, 2012
Due to the changes to the informed consent approval process and template, the eRA Versions folder for each study file will no longer contain the “Consent Form – Word Vers.” folder. All documents including the Word version of the informed consent document, assent, or parental permissions form are now located in the “Approved Documents” folder.
October 8, 2012
A new informed consent template has been released. Informed consent forms will no longer be stamped with an expiration date. The documents will still have an IRB approved date which will be located in the header of the document.
October 1, 2012
Amendment submission eForms have been replaced with the HRP-213: FORM - Amendment.
September 18, 2012
Study Closures are now called Final Reviews. Additionally, the associated eForm has been replaced with the HRP-212: FORM - Continuing/Final Review Progress Report.
September 18, 2012
Continuing Review submissions eForms have been replaced with the HRP-212: FORM - Continuing/Final Review Progress Report.
August 29, 2012
Continuing review reminders will only be sent out 60 and 30 days before expiration.
May 25, 2012
May 21, 2012
You are no longer required to attach study documents, including any informed consent documents or the protocol document with your Continuing Review submissions. The IRB office maintains copies of all approved study documents in eRA and will reference those documents during the review.