The medical device industry is shifting toward country-specific regulatory demands, in- country manufacturing and supply chains, and improved affordability of healthcare. This is requiring a significantly more complex approach to the development of the quality practices and procedures that ensure device quality and compliance known as design controls.
Teamcenter Design Control Executive
Abstract
What you get from this white paper
Key Features:
- Design activities and deliverables are specified in detail in a detailed design and development plan.
- Design reviews are documented.
- Documentation for validation.