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[R434.Ebook] Free PDF 21 CFR 11, 210/211, 820 with Audit Checklists - GMP Auditor's Basic Handbook (US Food & Drug Adminstration Title 21 CFR Parts), by Code of

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21 CFR 11, 210/211, 820 with Audit Checklists - GMP Auditor's Basic Handbook (US Food & Drug Adminstration Title 21 CFR Parts), by Code of

US FDA Title 21 CFR Parts Part 11 - Electronic Records/Electronic Signatures (ERES) Part 210/211 - cGMP in Manufacturing, Processing, Packaging or Holding of Drugs and Finished Pharmaceuticals Part 820 - Quality Systems Regulations Auditor's Check Lists Part 11 Electronic Systems Auditor's Checklist GMP Auditor's Checklist Quality Systems Regulation Auditor Checklist

  • Sales Rank: #2645107 in Books
  • Published on: 2014
  • Binding: Paperback
  • 220 pages

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