Do You Have An ISO 11607-01 Question?

With recent revisions to the ISO 11607 industry standard, many medical device manufacturers are unsure about how requirements for their package validation have changed.

The most revised section of the ISO 11607 standard is Clause 6, which focuses on a package's ability to deliver a medical device to the patient without jeopardizing sterility or incurring defect.

Join John Hart, CEO of DDL Inc., at MD&M Minneapolis 2006 for "ISO 11607 Revisions - Understanding Clause 6".

John will discuss the changes to Clause 6 and how medical device manufacturers and packaging professionals can prepare themselves for a package validation under ISO 11607-01.

          ISO 11607 Revisions - Understanding Clause 6
          Thursday, October 26 at 9 am
          Minneapolis Convention Center

DDL also invites you to submit an ISO 11607-01 related question to be answered by an expert DDL Package Engineer. 

Visit the DDL booth #849 at MD&M Minneapolis to receive an ISO 11607-01 FAQ of all questions submitted.

You can also listen to a series of ISO 11607 Revisions webinars on-demand.

Please submit your ISO 11607-01 question below by October 20, 2006.

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