DuPont Submission to U.S. FDA Fast Approaching the Finish Line 

DuPont Submission to U.S. FDA Fast Approaching the Finish Line

The latest in a series of webcasts about the DuPont™ Tyvek® Medical Packaging Transition Project (MPTP) was held on May 21st, 2015. During this webcast, DuPont experts shared the latest data and reports summarizing testing results across 100,000 packages from 55 medical device manufacturers globally. With about 80% of results in so far, the project is on track for submission to the U.S. FDA slated for this summer and commercialization beginning in the third quarter. They also discussed how functional equivalence supports interchangeability and provided updates on regulatory guidance. Slides shared during the webcast are available for download.