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Record Retention and Archival Policy

  • Post author:pharmabeginers
  • Post published:December 25, 2019
  • Post category:Audit/cGMP/Doc/QA Sop/SOPs
  • Post comments:3 Comments

The retention period for the Documents and Records in which record shall be retained /preserved in a facility according to their archival policy. The followings are the records and their…

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Document Management System

  • Post author:pharmabeginers
  • Post published:December 25, 2019
  • Post category:Doc/QA Sop/SOPs
  • Post comments:4 Comments

A document is a physical or digital representation of a body of information designed with the capacity (and usually intent) to communicate. Below the Standard Operating System (SOP) for Document…

Continue ReadingDocument Management System

Process Validation SOP and Protocol

  • Post author:pharmabeginers
  • Post published:December 21, 2019
  • Post category:cGMP/Protocol/QA Sop/SOPs/Validation
  • Post comments:5 Comments

Process Validation: Establishing documented evidence through collection and evaluation of data from the process design stage to routine production, which establishes scientific evidence and provides a high degree of assurance…

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Recent Posts

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