Category: Service Solutions

Service Solutions

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Case Study: Equipment Design with Service in Mind

Patient and user experience inspire clinical features, aesthetics, and other design elements for medical equipment. Similarly, it is important to take the product’s serviceability into consideration early in the design process to enable optimal uptime of that equipment throughout its lifecycle, which can have a significant impact on patient and user satisfaction.

The CompTIA HIT Exam: Narrowing the Gap Between IT and Biomed

At the Association for the Advancement of Medical Instrumentation’s recent annual conference, there was a lot of talk about closing the gap between IT and biomed. Certification is a key way to achieve this, Draeger’s IT technical trainer Joe Mitura says, and he shares tips for acing CompTIA’s HIT technician exam here.

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Setup and Long-Term Care for Clinical Workstations

Healthcare IT departments are increasingly deferring the support of clinical workstations to biomed teams. The biomed team now is often responsible not only for setting up the computer, but also for its long-term care. This article details maintenance issues and best practices teams can follow to help keep the clinical workstation functioning properly.

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ECRI Launches User Rating Tool for Medical Equipment Purchases

ECRI Institute has announced the launch of an online user review and rating tool for medical capital purchases that enables medical equipment users to share their opinions and assign ratings, helping hospitals and other healthcare providers make safe, cost-effective purchasing decisions. The Rate This Model tool is the latest addition to the SELECTplus suite of capital decision support services.

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Power Strips and RPTs—Where Are We Today?

There are several ways to meet the CMS protocol on power strips use in patient care areas, notes Pat Lynch. You can go out and buy hundreds of special relocatable power taps—or try a little creative thinking first.

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Principles and Methods of Testing Infusion Devices

Because infusion devices have been involved in a number of safety incidents in recent years, they must be regularly tested and evaluated to ensure that they are functioning to the manufacturer’s specification and within clinical and environmental expectations.

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