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    FDA's Problem with Software Monsters

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    Website https://www.traininng.com/webinar/fda's-problem-with-software-monsters-200597live?ourglocal_seo | Want to Edit it Edit Freely

    Category Online Professional Trainings;world class professionals trainings;professionals training courses;Online FDA trainings

    Deadline: February 04, 2019 | Date: February 05, 2019

    Venue/Country: Online, U.S.A

    Updated: 2019-01-09 16:17:30 (GMT+9)

    Call For Papers - CFP

    Overview

    Software's level of complexity and use keeps expanding at exponential levels. Likewise, the potential risks to health and loss of privacy follow suit. Ransomeware attacks hold software programs hostage until you pay the culprit thousands of dollars.

    Life supporting and life sustaining health software grinds to a halt. Extracting personal healthcare information is another plague that has a huge financial incentive for hackers. Your software is running on thin ice. FDA looks at software based on the risk to health associated with the software's use.

    Cybersecurity problems for software for life sustain devices, wireless networks for patient manage and home use devices open the gate for cyber intrusion, functional malware and total denial of access denial to an entire network of software, such as that used in hospitals and clinics. Who will help you? This becomes a self-help scenario; FDA and the FBI cannot protect you from the "bad guy." An equally disastrous problem involves interoperability failures.

    If your software does not cross the bridge of software communication, that software becomes worthless. Wireless technology, mobile apps and home use of software-based devices raise endless vulnerabilities. How you protect yourself and your customers in this swamp of disasters is critical.

    Why should you Attend

    FDA's regulatory controls

    Cybersecurity management

    Ransomware attacks and recovery

    Use voluntary standards and NIST

    Mobile apps

    Wireless/home use software systems

    Areas Covered in the Session

    Understand FDA's risk-based regulatory strategy

    Learn where FDA and you can find current technical help

    Highlight the problems of interoperability and what you can do about it

    Familiarize yourself with the National Institute of Standards and Technology's (NIST) role in cybersecurity prevention and interoperability considerations

    Learn about the FDA's increased use of voluntary standards

    Clarify FDA's ongoing revision of mobile app regulation

    Who Will Benefit

    Business Planning Executives

    Regulatory Directors

    Software Design and Specification Developers

    Real time Software Performance Auditors

    Recall Managers

    In-house Legal Counsel

    Customer Support and Service Directors

    Contract Specialists

    Business Acquisition Managers

    Hospital Risk Managers


    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.