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Update March 14, 2009

As part of quarterly scheduled updates, the following changes have been made in eIRB:
  • Continuing Review application - Study Population - the approved sample size from the application is listed as a read-only field.
  • Continuing Review application- Study Status - added an “other” option.
  • Continuing Review application – Finalize - no longer asks if a Change in Research or Protocol Event is also being submitted.
  • New page on the Change in Research application - displays the current approved no logo consent/assent forms to be used when making changes. These documents are read-only. Once an application has been converted to the new format, this page will disappear and the no logo forms can be found on the applicable consent/assent page.
  • Further Study Action pages are numbered.
  • Print Friendly View for Further Study Actions - displays study number and PI name.
  • New Application - Drug Information - added an upload field for a track changed version of the Investigator’s Brochure (if requested by the IRB).
  • New Application – Investigational Drug Service name changed to Drug Storage.
  • New application – Study Location - Johns Hopkins General Clinical Research Center (GCRC) name change to Johns Hopkins Institute for Clinical and Translation Research – Clinical Research Unit (ICTR-CRU).
  • An ID number is listed next to each study team member name. This is the identifier in eIRB and is not related to JHED or eIRB passwords.
  • Minor changes to electronic letter formatting and language.

If you have any questions, please contact the JHM eIRB at or 410-955-3008.