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Pharmaceutical Manufacturing and Packing Sourcer
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| The validation of disinfectants for use in controlled environments can be both lengthy and expensive. This article examines the scope of disinfectant validation and how to ensure a smooth and successful outcome. As a disinfectant manufacturer we have a unique perspective on validation as not only do we have an in-depth knowledge of disinfectants but we also operate cleanrooms to the same cGMP standards as pharmaceutical manufacturers. It also allows us to gain a broad range of experience across the many life science fields including the pharmaceutical, biotechnology and medical device industries where similar issues arise repeatedly. The message is simple: consider all aspects of new agents right from the start. This will produce quick and meaningful validation results, which subsequently leads to early implementation of new disinfectants and prompt responses to audits. |
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Industry Events |
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EMBALLAGE 2008. World Packaging Exhibition
16-21 November 2008, Paris-Nord Villepinte - France
“Business, Innovation, Outlook” are the watchwords for the 38th World Packaging Exhibition which opens in Paris from 17 to 21 November 2008. Fifteen months before the key packaging event of the end of 2008, EMBALLAGE displays its differences to offer you a new edition that is even more representative, international and rich in new features.
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