Manage ASME V&V 40 Standard Compliance with Ansys Minerva
Discover the Ansys solution for end-to-end credibility workflow for the ASME verification and validation process.
Time:
March 2, 2022
11 AM EST / 4 PM GMT / 9:30 PM IST
Venue:
Online
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About this Webinar
The ASME V&V 40 standard on "Verification and Validation" in Computational Modeling of Medical Devices" is an FDA-recognized 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 organization.
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 modeling data throughout the product development process.
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
Speakers:
Marc Horner, Senior Principal Application Engineer, Ansys
Rahul Ingle, Lead Consulting Engineer, Ansys
Ankur Jaura, Lead Consulting Engineer, Ansys
Angel Guzman, S&C Project Engineer Advisor, Standardization and Testing, ASME
See What Ansys Can Do For You
See What Ansys Can Do For You
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