At this stage, we launch the component into production, and Biomerics continues to assist you with post-launch quality assurance.
High-level outputs
- Determine medical device reporting (MDR) methodology to handle post-launch issues
- Obtain management approval to release the component to production
- Begin production
- Review plan for continuous improvement
Results
The Component Design management team approves the component for release to production. The Component Design team also signs off on the MDR methodology and plan for continuous improvement. We launch into production.
Tools
We use a detailed process—following established standard operating procedures and ISO requirements—to achieve management approval to release the component to production. After your component is in production, Biomerics continues to support you post-launch.
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