|
3. The
Testing Lab is ISO Registered
|
Contact
DDL by filling out the form below, email
us, or call
714-979-1712 to discuss an upcoming package or product
testing project.
|
|
|
"The difference
between using an ISO registered lab and one that
is not is huge when you are in the medical device
business. When it comes to the FDA, ISO registration
goes a long way during audits and submissions for
product approval."
JOHN GILKERSON
Project Manager, TherOx Inc.
|
|
Many labs are ISO compliant, however you should insist that your testing lab is ISO REGISTERED
ISO Registration means that the lab is required to:
- assure high quality testing processes
- develop documentation for each phase of the testing process
- partake in ongoing auditing
- commit many years to achieving registration
- apply for a certificate by a Notified
Body with a registration ID number
DDL recognizes that it is critical to achieve
and maintain ISO registration. We believe Engineers should insist
on an ISO registration from their package and product testing
lab.
Additionally, for detailed information on
how revisions to the ISO 11607 standard may affect the
testing of your packaging and business practices, please register
to attend an upcoming webinar "ISO
11607 Revisions" hosted by Patrick Nolan, member
of the ISO 11607 revision committee and COO of DDL.
Contact DDL by
filling out the form below, email
us, or call
714-979-1712 to discuss an upcoming package or product testing project. |
