Medical device packaging regulations have changed. The new ISO 11607-01 standard has just been published, bringing a change in compliance requirements for medical device manufacturers and packaging professionals.

DDL West understands that keeping abreadst of industry changes is difficult. This is why we are offering a series of free ISO 11607 Revisions Webinars to ensure that your medical device packaging does not fail when it enters the testing lab.

Attend Webinars 1 & 2 on-demand:
The New Revised ISO 11607-01
ISO 11607 Revisions - Understanding Clause 6

Register for the final Webinar in this series:
ISO 11607 Revisions - Implementing Clause 6

Choosing a package testing laboratory can be overwhelming, especially when dealing with packaging for critical medical devices.

How do you know whether you can trust your current medical device package and product testing laboratory? DDL West has put together a checklist outlining the key questions you should ask yourself about your current lab.

View the full newsletter here>

Sincerely,

Michael B. Foster
DDL West Package Engineer
VP & Treasurer of IOPP Southern CA Chapter

Created on Tuesday, June 20th, 2006 at 3:47 pm. | Fled under DDL West, DDL West, Newsletters. | Comment Feed