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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
Date: 2015-03-04 04:31:16
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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