Designated for groups developing medical device test systems (design validation, manufacturing test) or manufacturing automation with NI products, this new training course will teach you how to navigate regulatory requirements and business demands when using LabVIEW software for test and automation in regulatory markets.
Key objectives for this course include:
- Developing an understanding of the regulatory requirements in this area
- Exploring best practices for using standards and application life cycle processes
- Learning the GAMP 5 risk-based approach for developing test applications
- Examining NI tools and techniques to simplify testing and documentation requirements for your applications
>> Learn more about prerequisites and view the course outline here.