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Pharmaceutical industry / Validation / R / Title 21 CFR Part 11 / Good laboratory practice / Medical device / Good manufacturing practice / Clinical trial / Business process management / Software / Electronic trial master file


R: Regulatory Compliance and Validation Issues A Guidance Document for the Use of R in Regulated Clinical Trial Environments December 15, 2014
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Document Date: 2015-03-04 04:31:16


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File Size: 220,32 KB

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