Information on Case Reports
More frequently, individuals submitting case reports are asked to obtain the approval of the patient or patient's LAR for the information to be used in the report. This may be de-identified information or identifying information. Below is some information to help you in ensuring you are following the correct process and have the appropriate forms.
PLEASE NOTE: These forms and processes are not part of the IRB. The information is posted here as helpful information. If you have any questions, please see the noted point of contact for each item.
Patient Consent Form for A Case Study That Only Uses Deidentified Data
Questions about your obligation should be directed to the Privacy Officer where you work (or where the patient was treated) or, if you are a Macon & Joan Brock Virginia Health Sciences at Old Dominion University student, to evmsresearch@evms.edu.
Medical Group Patient Consent for Case Study That Contains PHI
Contact Leanne Smith or Shana Hollowell
Sentara Healthcare - Sentara Portal for Case Reports
Questions for the Sentara Health Research Center?
Email at research@sentara.com or call 1-833-866-7766