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.