Webinar Search Results : 2 Upcoming webinars found.
Thomas Bento Friday, July 20, 2018
10:00 AM PDT | 01:00 PM EDT
Duration:60 Minutes
Price: ¤150.00
by: Thomas Bento
The Value of a Human Factors Program
This webinar will explain the implementation of ISO 62366 and the regulatory expectations discussed in the 2016 FDA Guidance for a compliant human factors/ usability program.

Thomas Bento Friday, August 17, 2018
10:00 AM PDT | 01:00 PM EDT
Duration:60 Minutes
Price: ¤150.00
by: Thomas Bento
Validation of Non-Product Software
This course will teach how to comply to 21 CFR Part 820.70(i) and effectively implement a software validation program for medical devices, meeting the FDA requirements and produce a safe product. We will explain the role of Risk Management in Non-Product Validation. How software requirements are used in validation will be described.

  • Thomas Bento Recorded
    View Anytime
    Duration:60 Minutes
    Price: ¤190.00
    by: Thomas Bento
    The Value of a Human Factors Program
    This webinar will explain the implementation of ISO 62366 and the regulatory expectations discussed in the 2016 FDA Guidance for a compliant human factors/ usability program.

  • Thomas Bento Recorded
    View Anytime
    Duration:60 Minutes
    Price: ¤390.00
    by: Thomas Bento
    The Value of a Human Factors Program
    This webinar will explain the implementation of ISO 62366 and the regulatory expectations discussed in the 2016 FDA Guidance for a compliant human factors/ usability program.

  • Thomas Bento Recorded
    View Anytime
    Duration:60 Minutes
    Price: ¤190.00
    by: Thomas Bento
    The Value of a Human Factors Program
    This webinar will explain the implementation of ISO 62366 and the regulatory expectations discussed in the 2016 FDA Guidance for a compliant human factors/ usability program.

  • Thomas Bento Recorded
    View Anytime
    Price: ¤390.00
    by: Thomas Bento
    The Value of a Human Factors Program
    This webinar will explain the implementation of ISO 62366 and the regulatory expectations discussed in the 2016 FDA Guidance for a compliant human factors/ usability program.

  • Thomas Bento Recorded
    View Anytime
    Price: ¤190.00
    by: Thomas Bento
    Validation of Non-Product Software
    This course will teach how to comply to 21 CFR Part 820.70(i) and effectively implement a software validation program for medical devices, meeting the FDA requirements and produce a safe product. We will explain the role of Risk Management in Non-Product Validation. How software requirements are used in validation will be described.

  • Thomas Bento Recorded
    View Anytime
    Price: ¤390.00
    by: Thomas Bento
    Validation of Non-Product Software
    This course will teach how to comply to 21 CFR Part 820.70(i) and effectively implement a software validation program for medical devices, meeting the FDA requirements and produce a safe product. We will explain the role of Risk Management in Non-Product Validation. How software requirements are used in validation will be described.

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Fremont, CA 94539, USA.

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