Hello,
I am trying to gain some insight from other Medication Safety Officers regarding how they interact with the IRB and investigational drug services.
Typically errors that occur in this space are documented as study variances and are addressed by the IRB. Do any of your sites also ask that these errors be reported internally to the hospital's voluntary error reporting system for further review?
Thank you in advance for your responses!
Sincerely,
Bridget Gegorski, Pharm.D.
Medication Safety Officer
University Hospitals Office: 216-983-1307
11100 Euclid Ave Fax: 216-844-3052
Cleveland, Ohio 44106 Mail Stop: WRN 5006
Bridget.Gegorski@UHHospitals.org