Akron, Ohio - For medical device manufacturers, an 11-13 June conference organised by Plastics News will have a session helping assess how to gain FDA approval.
At Plastics in Medical Devices 2012, being held in Westlake, Ohio, attendees will get the perspectives of two lawyers and a plastics industry expert on the tricky FDA approval process.
Len Czuba of Czuba Enterprises Inc., Rick Stearns of Keller & Heckman LLP, and Andrew Cox from Thompson Hine LLP, will discuss the FDA regulatory environment including biomaterial supplier liability issues and managing risk. Solo presentations will be followed by a panel discussion.
The organiser claims that Plastics in Medical Devices North America is the networking event for the medical device industry, connecting all parts of the supply chain.
Attendees will get advice on hot-button topics in the medical device manufacturing industry, including offshoring, value-driven engineering, regulatory issues, material and application advances, device design trends, and how the plastics industry is working to combat hospital-acquired infections,"
See more at www.plasticsnews.com/pmd2012