Part 11 and Computer Validation GuidebookUniversityOfHealthCare, 2005 - 323 lappuses Gives an introduction to computer issues in the pharmaceutical industry, as well as to computer systems validation. This work helps you learn about regulations, the personnel responsible for computer validation, how to accomplish validation, examples of regulatory problems, and more. It is useful for research personnel in FDA-regulated industries. |
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... Clinical Trials and GCP ( Good Clinical Practices ) , GMP Training Introduction To Meet FDA Regulations in the Use of Computers in Pharmaceutical , Medical Device , Food , and Cosmet- ics Manufacturing 000 Daniel Farb , M.D. Bruce ...
... Clinical Trials and GCP ( Good Clinical Practices ) , GMP Training Introduction To Meet FDA Regulations in the Use of Computers in Pharmaceutical , Medical Device , Food , and Cosmet- ics Manufacturing 000 Daniel Farb , M.D. Bruce ...
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... Guidance for Industry on Software Validation 249 Compliance Policy Guide 160.850 266 Computerized Systems in Clinical Trials 271 21 CFR PART 58 279 21 CFR Part 210 and 211 298 Introduction This book is a text-only version of the acclaimed.
... Guidance for Industry on Software Validation 249 Compliance Policy Guide 160.850 266 Computerized Systems in Clinical Trials 271 21 CFR PART 58 279 21 CFR Part 210 and 211 298 Introduction This book is a text-only version of the acclaimed.
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