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Whitepaper
Turnkey Modular Manufacturing
With the recent downswing in the economy, as well as the current uncertainty about the affect of healthcare reform policy on the medical device and pharmaceutical industries, finding ways to improve efficiency and control costs has never been more important for manufacturers.
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Whitepaper
What's your IQ OQ PQ validation IQ?
When it comes to packaging systems used for terminally sterilized medical devices, preserving sterility until use can literally be a matter of life and death. That’s why it’s so important for medical device manufacturers (MDMs) to ensure that the forming, sealing and assembly of sterile barrier systems (as well as the sterile barrier systems themselves) meet ISO 11607-2 requirements for IQ OQ PQ validation.
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