Many hospitals already use the eFilm Workstation for their radiologists to view studies stored on their hospital PACS (Picture Archiving and Communication System).ĮFilm Mobile HD allows users to (Figures 15-18): Is licensed by Health Canada and bears the CE Mark for distribution in Europe. ResolutionMD Mobile received 510(k) clearance from the U.S.įood & Drug Administration (FDA) in September 2011,

2D (dynamic win/lvl and viewing presets).

Standard features include (Figures 9-14): It is 100 percent secure.” says Bryon Osing, With only a tiny trickle of data feeding the device to create the output on the screen. “All images/data are rendered on the server side,Īnd application is virtually presented on the handheld device.

access to full suite of rendering tools.

elimination of security concerns (information and images stays in the server room).This application provides numerous benefits including:

This app requires access to a configured ResolutionMD Server via a wireless connection (Wi-Fi or 3G).īecause the confidential patient information or data is never retained on the mobile device, ResolutionMD Mobile (Calgary Scientific): Navigation among series is performed with a quick flick across the screen. The Standardized Uptake Value (SUV – which quantifies glycolytic activity) (Figures 2-8). You can access images from any internet connection,Įnhancing teleradiology and multi-institution reading operations.Īdditional viewing features include distance measurement,Īn ROI measurement which allows for the radiodensity of a portion of the image to be measured in “Hounsefiled” units or in the case of PET studies, One feature that sets MIM apart is that it offers MIMCloud,Ĭloud-based DICOM service that makes storage and sharing of imaging studies very simple. Radiology images taken in the hospital or physician’s office are compressed for secure network transfer then sent to the iPad via software called Mobile MIM. Mobile MIM has also been approved for diagnostic X-ray and ultrasound viewing in most recent FDA review.Īnd the application is indicated for use only when there is no access to a workstation, The FDA also reviewed results from demonstration studies with qualified radiologists under different lighting conditions.Īll participants agreed that the iPad was sufficient for diagnostic image interpretation under the recommended lighting conditions.Īfter the first FDA approval they received in February ’11,

The FDA reviewed performance test results on various portable devices.Īnd noise in accordance with international standards and guidelines. Such as positron emission tomography (PET). Mobile MIM app was the first system approved by the FDA for viewing images and making medical diagnoses based on computed tomography (CT),

Efilm lite to viw mri