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21 CFR Part 11 : Electronic Records & Signatures

  • Post author:pharmabeginers
  • Post published:September 13, 2021
  • Post category:Audit/cGMP/IT SOP/QA Sop/QC Sop/SOPs
  • Post comments:0 Comments

Guideline (SOP) for Electronic Records & Signatures (21 cfr part 11) and implementation of the same during Data generation and assurance at pharmaceutical drug manufacturing plant and API. 21 CFR…

Continue Reading21 CFR Part 11 : Electronic Records & Signatures

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