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Medical devices

In general, software verification and validation (V&V) is the process of checking that a software system meets specifications and fulfils its intended purpose. Developers, testers and users are essential parts of the software development lifecycle. V&V is utilized to ensure that the software achieves its intended use without bugs or gaps. It is essential to understand the software relevant standards and regulatory requirements and fulfil these requirements throughout the development and testing of software system. This webinar will introduce you to these standards and regulations requirements and highlight the important points that you need to be aware of them when developing and testing software systems for medical device.

Medical Device Software Verification and Validation

Download the slides for the June 23, 2020 Webinar

Medical Device Software Verification and Validation Presentation Materials

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