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.


Learn from the following experts:

Greg Moakes

Senior Manager Field Development

Greg Moakes leads the US Medical Field Development Team. His team partner with designers and design engineers to select the optimal materials for their medical and pharmaceutical devices and dosage forms. Greg joined Celanese in 2007 and has held multiple roles in procurement, business development, sales, and technical leadership. Greg holds a Ph.D in Electroanalytical Chemistry from Georgia Tech and an MBA from SMU in Dallas.