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Manage ASME V&V 40 Standard Compliance with Ansys Minerva | Ansys Webinar
  • 2nd March 2022
    4:00 pm - 5:00 pm

2 March 2022

4 PM GMT 

The ASME V&V 40 standard on “Verification and Validation” in Computational Modeling of Medical Devices” is an FDA-recognised standard that guides users in establishing and assessing the verification, validation, and uncertainty quantification requirements of computational models for a specific context of use. However, implementing and then documenting the various credibility requirements and associated credibility activities can be time-consuming and lack consistency, traceability, and security within the organisation.

 

To address these needs, Ansys recently developed a template-based, end-to-end credibility workflow that guides users through the ASME V&V 40 standard procedure in a logical manner. This template can track all aspects of model development, from identifying credibility requirements to defining simulation work requests to communicating with internal stakeholders. This solution manages the digital thread for computational modelling data throughout the product development process.

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Simply choose one of the following options to receive further information or to register.

Please note that this event is free to attend but registration is essential. If you are unable to attend the webinar, please register to receive a copy of the recording when it becomes available.

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Details on how to join the webinar will be emailed to you once registered.

What Attendees Will Learn

  • Tour the Ansys Minerva simulation process and data management (SPDM) platform
  • Learn how Ansys MInerva supports medical device industry requirements, such as CFR Part 11
  • Watch a demo of the ASME-40 template in Ansys Minerva

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