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
Prerequisites
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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