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Using NI LabVIEW for Test and Automation in Regulated Markets

Course Overview
Learn to navigate regulatory requirements and business demands when using NI LabVIEW software for test and automation in regulatory markets, specifically in regulated medical device test. Also explore best practices for design validation and manufacturing test using a fictional example of a medical device manufacturing test fixture, maintained throughout the course to illustrate concepts and provide a basis for discussion. By incorporating these efficient and reliable development processes, you can address business and regulatory risk considerations while ensuring the success of any test and automation project you are developing.
Key Objectives
  • Develop an understanding of the regulatory requirements in this area
  • Explore best practices for using standards and application life cycle processes
  • Learn the GAMP 5 risk-based approach for developing test applications
  • Examine NI tools and techniques to simplify testing and documentation requirements for your applications
Additional Information

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Who Should Attend

Groups developing medical device test systems (design validation, manufacturing test) or manufacturing automation with NI products


Experience with NI test system development. Some understanding of medical device test applications. LabVIEW Core 3 or experience developing medium to large LabVIEW applications.

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NI Training Credits are designed for individuals and companies that want to purchase training for multiple employees or team members but need the flexibility to decide who participates in the training and discuss scheduling. Credits are valid for one year after purchase. Buy Now

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States or RegionsFormatCourse LanguageStart Date and TimeCourse LengthTraining CreditsPrice
FORT WORTH, TX Classroom English May 18, 2015 8:30 AM CDT 2-days 5$ 1,689
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