FSI, a leading health care CMMS/EAM provider, has announced an integration with Fluke Biomedical OneQA workflow automation software to bring enhanced efficiency and accuracy to device testing workflows. Offering this innovative approach for the market creates an integration that adds value and usability to launch OneQA device testing from within a CMS work order. Results are automatically recorded, reducing manual data entry and time spent utilizing separate platforms.
OneQA software seamlessly works in tandem with FSI’s CMMS to reduce duplication in device testing for biomedical professionals. The partnership addresses areas that commonly cause frustration in the management of device testing, such as:
- Delays in work orders that require device testing and documentation between two systems
- Clunky data entry processes and inaccurate reporting
- Friction in preventive maintenance, equipment reliability, and compliance workflows
“We are looking forward to seeing how the device testing experience changes for OneQA users from utilizing this new capability. Integrating with FSI is bringing a frictionless experience in using OneQA software, allowing users to test and record data from within an associated work order without having to switch platforms or manually enter information,” said Jeremy Olson, Director, Product Management (EQA), Fluke Health Solutions.
The OneQA integration is the latest development in FSI’s work to ensure software compatibility and optimized workflows with the tools users rely on most frequently. Introducing integrations focused on compatibility with top tools allows more time and energy to be spent on maintaining a functional health care environment rather than on manually recording and managing CMMS data. Leveraging this integration both minimizes time needed to complete device testing workflows and adds a layer of data accuracy that supports widespread functions in healthcare maintenance management.
“Fluke Biomedical OneQA software is a tool that we have heard being utilized by many of FSI’s biomed users, and we are excited to introduce an integration that adds efficiency and reduces the margin of error in managing device testing data. Users with this integration are able to launch OneQA, run testing, display and record results all without leaving a work order,” said Chris Lang, Vice President of Product and Strategy, FSI.
The FSI Product and Customer Success teams are committed to offering a variety of integrations that support HTM professionals with improving data integrity, reducing time spent on manual workflow steps, and adding efficiencies that keep the focus on the work that matters most, not on frustrating processes.
After spending in-person time at numerous events and AAMI eXchange listening to priorities for HTM users, the FSI product roadmap and integrations strategy continues to evolve and exceed the needs of the HTM professional.
Find out more at MD Expo by visiting FSI at Booth 214.
