Packaging

White Paper Explains Package Validation Requirements For Medical Devices & Combinatory Products

Wednesday 10. June 2009 - Validation requirements and combination products pose a unique set of challenges to the medical device engineer. A new whitepaper from Microtest Laboratories discusses how an engineer can best to utilize packaging validation programs and discusses options when testing medical device packaging.

The white paper, “Package Validation Requirements For Medical Devices and Combinatory Products” provides an insight into the general requirements in microbiological and physical testing programs.

Specifically, the white paper discusses that medical device stability package validation programs should be designed to encompass the overt product storage and shipment conditions and that performing accelerated aging studies does little to address liability during shipment and storage.

The white paper discusses:
— The necessity to develop a robust packaging validation regimen
— That a packaging validation program should include transportation
simulation testing with concomitant sterility testing.

— A comprehensive regulatory approach to validation during early product
development can save many weeks of redevelopment and testing
activities.



The white paper is authored by Steven Richter, Ph.D., is President and Chief Scientific Officer of Microtest Laboratories, (www.microtestlabs.com), a contract manufacturer and provider of contract manufacturing testing.

Or, visit Microtest at the 2009 MD&M East, June 9th-11th, in Booth 1442 in the Jacob K. Javitz Convention Center New York, NY.