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Packaging Validation

September 6, 2017

Three-Day Webinar Series: Medical Device and Pharmaceutical Testing Regulatory Updates, Trends, and Anticipated Changes

Learn from the industry-leading experts at Nelson Laboratories in the three-day webinar series Medical Device and Pharmaceutical Testing Regulatory Updates, Trends, and Anticipated Changes including FDA, ISO, USP, and MDRs. The experts at Nelson Labs are teaming with MD+DI to...

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February 3, 2016

Non-Porous Packaging Validation

Over the past few years, as medical device manufacturers look for new and innovative ways to package, sterilize, and market their products, the use of non-porous materials in packaging has become more and more popular. Similar to porous packaging, non-porous...

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April 13, 2015

DuPont’s Tyvek Transition: Are You Prepared?

With DuPont’s Tyvek transition looming, manufacturers should consider performing a packaging validation as part of their implementation strategy. Nelson Laboratories has been working with the new Tyvek material, testing it according to the ASTM F2638 method, for several years. DuPont...

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October 28, 2014

ISO 16775: The Medical Device Packaging Professional’s Latest “Must Have”

If you are involved in the packaging of medical devices, your primary standards reference has probably been the International Organization for Standardization (ISO) 11607 publication for packaging design and validation. However, this standard was lacking much of the detail and...

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May 12, 2014

ASTM Committee Meeting Updates for F02 and D10

Robert Haley, Packaging Department Manager, Nelson Labs The American Society for Testing and Materials International (ASTM) Committee Meeting for F02 and D10 committees was recently held in Lansing, Michigan.  During the F02 meeting, there were discussions for potential round robin...

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