MQSA EQUIP Module
In response to the new FDA requirements, MagView has introduced the MagView EQUIP Module, which can help your facility comply with the new FDA requirements in the most efficient way. The EQUIP Module includes the following features:
The Image Review Worklist allows the radiologist to review sample images as required, document deficiencies and indicate required corrective action.
The Corrective Action Worklist allows the technologist to review films which have been selected by the radiologist for corrective action and document the appropriate corrective action.
The Compliance Report allows the lead interpreting physician to report on the image review and corrective action for a date range as required by the EQUIP program.
For more information about the EQUIP Module and how it can prevent your facility from receiving reimbursement penalties, please contact your account manager.
Like the Post? Do share with your Friends.
When it comes to breast cancer risk, breast density is a known factor that can increase the difficulty of detecting an a...
A recent article published by Diagnostic Imaging highlights four cases of patients presenting with seemingly telltale in...
A common challenge for breast imaging centers is finding an effective strategy to get patients to return for their annua...