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    FDA's Medical Device Software Regulation Strategy

    View: 1564

    Website | Edit Freely


    Deadline: November 09, 2020 | Date: November 19, 2020-November 20, 2020

    Venue/Country: Boston, MA, U.S.A

    Updated: 2020-02-13 22:10:47 (GMT+9)

    Call For Papers - CFP

    The growth of the medical software industry outpaces the design of FDA's regulatory process. In some instances clinicians have weighed the risk of software failure against the benefits of using a device at all. Device software is often used in conjunction with other software-based devices, but their interoperability was never anticipated.

    How can you anticipate and defend against the malicious remote hacking and shut down of an insulin infusion pump?

    Can one software program defeat the performance capability or back up safety features of another software program?

    When interoperability surface, which software manufacturer takes the lead to solve the problem and deal with proprietary software issues?

    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.