Overseeing the "Tissue/Bone" program is the interpretation that our Medical Director has chosen. Not Responsible for the program. The reason for this is a practical one. We currently only store and issue Bone/Tissue, as we have the only freezer that gets cold enough to store it and comply with that need. Also the blood bank computer system module allows for the "Birth to Death" tracking needed, especially if there is a recall Storage and issuing was all we wanted to do, however, the new JCAHO guidelines came out and the OR, needless to say was no where neer compliant. Training? Competency checks? ANNUALLY - what do you mean by a monitored storage device? Acceptable supplier? The only part that hey were familiar with was the Acceptance protocol for the receipt of the ordered products before giving them to us to store. Our acceptance check list was modified for the receipt of Bone/Tissue and the BB wil not accept a piece of Bone/tissue for storage unless a copy accompanies the product. Thus at the request of our QA department, a Protocol delineating the responsibility of each party has been specifically stated and SOP's put in place to assure compliance. Utilization review - amount and type used/outdated, storage problems etc - is put into a report and presented at OR meeting and semiannual Transfusion committee Meetings. Any SOP changes have to be reviewed and signed by responsible QA departmental committees. Good Luck - This can of worms is bottomless and dealing with non-focused nursing staff is the biggest challenge. The not my job - your job, attitude wears thin and communication on all levels is needed.