Medical Design Technology

Article Summary

As medical device manufacturer’s face increasingly tougher scrutiny from regulatory agencies, they must do what they can to prevent possible causes for a rejection. This means ensuring the approval of every aspect of the submission, including the packaging. This month’s “View from the Top” speaks with [Pat Nolan, COO of DDL, Inc,] an expert on package testing and validation.

Created on Saturday, July 1st, 2006 at 3:18 pm. | Fled under DDL, Media Coverage. | Comment Feed