Medical packaging validating

For example, the site cannot determine your email name unless you choose to type it.Allowing a website to create a cookie does not give that or any other site access to the rest of your computer, and only the site that created the cookie can read it.By establishing product families, QTS can help minimize testing costs.


Still, many companies fail to develop an adequate validation program, which can prove costly if discovered by an inspector.Over the last several years, inadequate validation has been one of the most common sources of US FDA Form 483 findings, so it is critical to address this requirement early.Responding to a FDA Form 483 from the US FDA is disruptive and expensive, but can be much more so if major changes are required to retroactively validate a process, system, piece of equipment or working environment.Medical packaging can lose its integrity as a result of dynamic events that occur during processing and/or distribution.

Because of this, QTS employs physical test methods that validate the package integrity has been maintained throughout all the phases of processing, handling and expected shelf life.

Validation is broadly applied across the organization to ensure that products, equipment, processes, software and systems operate as designed and intended.


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