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According to GMP guidelines, pharmaceutical companies are required to validate processes that influence product quality. The applied machines and plants are subjected to a rigid qualification process. During this qualification it is tested and documented that the pre-specified functionality is achieved. As early as in the planning stages, IKA machines and units are designed to be suitable for use in the pharmaceutical industry.

IKA will provide the necessary documentation and, if desired, will conduct the design, installation and operation qualification with you.

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