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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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