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    ONLINE 2018 - Medical Device cybersecurity following latest FDA Guidance

    View: 137

    Website https://www.compliancetrainingpanel.com/Webinar/Topic?WB=MD00118 | Want to Edit it Edit Freely

    Category Online

    Deadline: November 28, 2018 | Date: November 28, 2018

    Venue/Country: usa, U.S.A

    Updated: 2018-11-16 13:25:46 (GMT+9)

    Call For Papers - CFP

    Description :

    The company must establish a program where they identify, analyze and control cybersecurity risks for both pre market and post market. The cybersecurity program must be carefully planned. A formal special hazard analysis must be conducted for each risk. Communication of risks must be sent to device users. A complex set of reporting requirements has been established. This webinar will describe a program that will be compliant to the FDA requirements.

    Why :

    Medical device cybersecurity has become very important to the FDA. They have recently issued two Guidance’s on the subject; the latest in December of 2016. FDA expects a proactive extensive risk based program to minimize risk to the user from cyber attacks including active involvement with information sharing groups.

    Areas Covered in the Session :

    • Cybersecurity plan

    • Risk based analysis

    • Hazard analysis following ISO14971

    • Risk communication to users

    • Required membership in information sharing groups

    • Reporting requirements and the exceptions

    Who Will Benefit:

    • company management

    • IT personnel

    • Development Engineers

    • Production Management

    • QA/ QC personnel

    • Software developers

    About Speaker:

    Edwin Waldbusser retired from industry after 20 years in management of development of medical device products and development of company Quality Systems. Products included IVD devices, kidney dialysis systems and inhalation devices. QS experience includes design control, risk analysis, CAPA, software validation, supplier qualification/ control and manufacturing/ non-conforming product programs.

    Edwin Waldbusser has a B.S. Mechanical Engineering from NYU and a M.B.A from Drexel University. He is certified by Lloyds of London as an ISO 9000 Lead Auditor and is a member of the Thomson Reuters Expert Witness network. He has 5 issued patents.

    Venue: Online

    Speaker Name:Edwin Wald busser

    Priice : $ 229

    Wednesday Nov28 , 2018

    EST 13:00

    Duration : 60 Minutes

    Email:supportatcompliancetrainingpanel.com


    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.