Equipamento médico novo e usado, equipamento do hospital, Auctions médicos do instrumento For Sale, e Wanted

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Philips Multi-Vendor Service - Clinical assets readiness, and more

Discover how Philips MVS has positioned itself as an invaluable resource for providers

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The secret to the ultimate biomed cart

Mass General CBET Scot Mackeil shares insight on the 'needed' and the 'nice-to-haves'

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AI software for cardiac echo could help in COVID-19 fight

Ultromics partners with Mayo Clinic for rapidly assessing heart disease

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US hospital operating margins plummet 282%, says new study

Surgery volumes declined the most, due to delays of non-urgent procedures

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PETNET Solutions and Zionexa get approval for breast cancer-specific PET imaging agent

Cerianna is the first FDA approved F-18 oncology PET agent since 2016

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Draft standard on refurbishing equipment could lead to greater manufacturer control

How the draft IEC standard 63120 could lead to OEM approval requirements

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United Imaging gets clearance for ultra wide 75-cm bore MR scanner

The uMR OMEGA is designed for obese and claustrophobic patients

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Getting ahead in HTM

Discover the skills, advice, and personality traits that leaders in the industry say make all the difference for becoming a successful team leader

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US government, private sector in talks to establish pandemic supply base

Creating a 'transparent organizing mechanism' for manufacturing and distributing supplies in future crises

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RSNA announces 2020 meeting will be held 'virtually'

Physical meeting being cancelled for first time since 1945

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Imaging volumes across patient settings and imaging modalities on steep decline

Scans decreased by 28% at Northwell Health in New York over 7-week period

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Less than half of DXA facilities surveyed adhere to quality assurance procedures

Of 121 international facilities, 25% were not accredited by professional or government organizations

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AdvaMed and MITA exit collaboration with non-OEM service stakeholders

Lack of progress and consensus contributed to departure from FDA-recommended group

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European Commission MDR implementation update: delayed but in process

Understanding periodic safety reports and postmarket surveillance, as well as the new database of medical devices

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HCBN Resource Guide

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