Medical Device Software: Verification, Validation & Compliance
Duration: 75 Minutes
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Software design is a complex set of interactions within the device, with the connecting devices, and with users of the device. Usually multiple factors affect the device performance. Therefore right validation is the key to prevent device recalls. The software associated with medical devices is getting closer scrutiny than ever before because of increasing prevalence in industry, greater chance for problems, and the comfort level of FDA investigators in asking for and auditing software applications.
12/07/2017 11:30 AM12/07/2017 05:30 PMTraining Topic: Medical Device Software: Verification, Validation & ComplianceInstructor: Nancy J. Knettell
This webinar will teach you how to design, build and test medical device software in preparation for the successful 510k submissions. It will cover medical device software user requirements, software architecture, design, unit testing and more.
Objectives of the Presentation
FDA Quality System Requirements for software
FDA guidelines on software verification and validation
Smart software verification methods
How to design smart validation tests
How to conduct black box testing and white box testing to perform thorough validation
How to conduct diabolic tests and wicked tests to avoid product recalls
Why Should you Attend
This webinar is essential for medical device companies interested in submitting software enabled medical devices or software as a medical device to the FDA for 510K approval. One of the biggest risks most company's face when submitting their device for approval is finding out after seven or more months of waiting that the 510K has been denied because the software portion of the submittal is inadequate and not compliant.
This webinar will ensure that device companies will know exactly what documentation needs to be prepared so the software portion of the submittal will be in compliance preventing delays of the 510K approval.
Companies can also face potential audit risks and serious findings post submittal that can block their ability to ultimately sell their product successfully. This course will ensure that you know what is expected to have in place for compliance for your company during the preparation of a 510K to prevent this risk.