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An Overview Of Package Integrity For Medical Device Manufacturers
Source: MOCON, Inc.
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Presentation: An Overview Of Package Integrity For Medical Device Manufacturers
What is Package Integrity?
- As defined in ASTM F-1327-05, Standard Terminology Relating to Barrier Materials for Medical Packaging….
- Package integrity is "the physical capability of a given package to protect its contents with the desired level of protection over a defined period of service; for example, as a barrier to physical, microbiological, or chemical challenges."
This presentation will answer several questions, including what package integrity is, why test for package integrity, and how to test for package integrity. It will also determine how to meet the new requirements of ISO 11607 Part 1 and Part 2 and will explain what TIR 22 is and what role the test method validation plays.
Click Here To Download:Presentation: An Overview Of Package Integrity For Medical Device Manufacturers



