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Nassau University Medical Center library undergoes $700,000 renovation

2014-10-09 21:56:00| American School & University

Located in the low-rise section of NUMCs Dynamic Care Building in East Meadow, N.Y., the library primarily supports the patient care, biomedical research and graduate medical education information needs of the medical staff, faculty and students read more

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Wireless Medical Technologies: Navigating Government Regulation In The New Medical Age

2014-10-08 17:35:29| rfglobalnet Home Page

Unless regulatory issues are taken into account at the earliest stages of the research and development process, device manufacturers could find themselves investing significant time and resources in products for which they cannot obtain government approval. In the U.S., three federal agencies, the Federal Communications Commission (FCC), the Food and Drug Administration (FDA), and the Centers for Medicare and Medicaid Services (CMS), are charged with regulating wireless medical devices. This article provides a comprehensive analysis of this tri-partite federal regulatory structure in order to help manufacturers navigate the myriad of technical rules and policies enforced by agencies with different, and sometimes divergent, objectives.

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U.S. medical workers get a crash coursea on Ebola treatment

2014-10-08 15:07:14| Biotech - Topix.net

TREATMENT: Centers for Disease Control and Prevention instructor Satish Pillai gives guidance to Paul Reed , chief medical officer for the U.S. Public Health Service, and Roseda Marshall, chairman of pediatrics at the University of Liberia's A.M. Dogliotti College of Medicine, in preparation for the response to the current Ebola outbreak, during a CDC safety training course in Anniston, Alabama, Oct. 6. ANNISTON Ala. - Dr. Kwan Kew Lai's family and colleagues in Boston fear for the safety of the infectious disease physician when she travels to Liberia later this month to treat Ebola patients.

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FDA Aims to Shore Up Medical Device Cybersecurity

2014-10-06 16:00:00| TechNewsWorld

The Food and Drug Administration last week released long-awaited recommendations aimed at better managing cybersecurity risks to protect patient health and information. The new standards recommend manufacturers take into account cybersecurity risks as part of the design and development of a medical device. They require device makers to submit documentation to the FDA about identified risks.

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Becton Dickinson to pay $12.2B to acquire medical equipment rival Carefusion

2014-10-06 04:18:40| Biotech - Topix.net

New Jersey medical equipment maker Becton Dickinson and Co. says it will pay $12.2 billion for rival Carefusion in a combination focused on medication systems for hospitals and pharmacies.

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