Webinar
Ultrasound technology has increasingly more and more uses from detection and diagnosis to intervention. Hospitals and health systems must maintain delicate and expensive ultrasound probes to ensure equipment is in top working condition for ultimate care and optimum uptime.
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VP of Quality, Jina Tweed, provides expert commentary on the release of the FDA's May 2018 Report of Safety and Effectiveness of Medical Devices. The Agency ruled they will not impose more regulations. Here’s what they will do instead.
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Ted Courtemanche and Dan Brenner share time benchmarks from top hospitals. Learn how your hospital compares and understand your team’s true costs of parts sourcing so you can improve efficiencies.
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Steve Kelley shares standard operating procedures and practical guidance on how you can implement a PM program that highlights safety and reduces the risk of using unsafe medical equipment.
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Great quality enables sustainable growth for an organization. There are several key performance indicators (KPIs) that healthcare organizations can use to measure and monitor the quality of medical device parts and the suppliers that provide them.
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During this presentation, you will learn the fundamentals of driving process and technology for an effective clinical engineering supply chain strategy.
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Clinical engineering teams frequently send assets out for depot repair and are responsible for the quality performance of each asset. But healthcare organizations often lose control and insight once an asset leaves the building. By implementing best practices, technicians and engineers can gain back control and transparency over depot repair.
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During this session attendees will learn: 1) The warning signs that departmental change is needed 2) Plan your work and work your plan - Best practices to manage a large-scale change 3) Building benchmarks - Managing checkpoints and achieving on-going success
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Recently, the servicing of medical devices has been evaluated for quality by the FDA. The Agency ruled that while they will not impose more regulations on third-party service providers of medical devices, they will foster evidence development to assess the quality, safety and effectiveness of medical device servicing and they will push for more providers to have Quality Management Systems (QMS) in place.
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