The regulatory landscape for medical devices is fluid. As such, suppliers must work to ensure that the innovations in material science that broaden design options are not adding additional risk to the development pipeline.
Our experts will discuss:
- De-risking part validation
- End-to-end support - the role of prototyping, processing and computer-aided engineering
- Customization and the medical compliance of materials
View our web seminar to discover how our experts can support your medical applications with complex requirements. Learn more about how early collaboration with Celanese in your next development can help you innovate whilst controlling risk.