Cleanroom Design and Validation Procedure
$149.00
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The cleanroom design and validation procedure provides instructions on the design, build, and validation of cleanrooms. User requirement specifications ensure the environment complies with applicable standards and regulations and the facility is fit for its intended purpose. The cleanroom design and validation procedure complies with the quality management system requirements of ISO 13485, MDR 2017/745, and FDA QSR. The document is in MS Word format and can be modified to meet your particular use case.
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