Validation Technology In recent years, there has been considerable growth in the demand for more sophisticated Clean Rooms. Many industries are beginning to discover the benefits of Clean Room technology, while other industries are developing their products in such a way that contamination control is becoming more stringent. This is more prevalent for the biotechnology industries where a few kilograms or even grams of product may be worth millions of dollars.Over the last twenty years, the demand for contamination control has increased to such an extent that the present state-of-the-art Clean Rooms are a thousand times cleaner than those designed in the past. Clean Rooms have progressively developed, and the stage has been reached where it is now possible to design a Clean Room to fulfill almost any environmental requirement..
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validation refers to establishing documented evidence that a process or system, when operated within established parameters, can perform effectively and reproducibly to produce a medicinal product meeting its pre-determined specifications and quality attributes
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Pharmaceutical Validation Documentation Requirements
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K. Dashora, D. Singh, Swarnlata Saraf and S. Saraf *. Institute of Pharmacy, Pt.RavishankarShuklaUniversity, Raipur 492 010. *Author for ...
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Thanks for sharing information
Cleanroom Solutions Hyderabad & Cleanroom Equipment in India
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