Packaging Testing Articles & Analysis
4 articles found
Therefore, medical device manufacturers consider four factors to reach a final medical device shelf life determination following FDA and ISO medical device shelf life standards. Packaging Through rigorous testing and analysis, packaging engineers and designers can determine how long a medical device will remain stable and effective within its ...
Packaging Validation Process The FDA and ISO 11607 require manufacturers to conduct validation testing in several areas, including: Accelerated Aging: These tests examine the sterile integrity of packaging materials over an accelerated period of time. ...
Planning the End Result from the Beginning Defining an optical device encompasses the creation of the design specifications, development of a realistic budget, avoidance of mechanical interferences while minimizing the packaging volume, manufacturability, test protocols for every stage, and ensuring that the desired features do not overshadow the critical ...
The packaging volume can be manufactured according to needs, and paper packaging can be recycled. ...