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.
- Overview: Regulations, Standards, Guidelines
- Life-Cycle Processes
- Test Equipment Life-Cycle Activities
- Operation Phase
- Retirement Phase