Audit

Audit Calibration GLP Quality Control SOPs
  • February 1, 2020
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SOP for Internal and External Calibration of Instrument

Standard Operating Procedure for Laboratory Instrument and Equipment calibration through Internal or External (Third Party). This SOP includes the calibration.

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Audit Checklist Checklist / Formats Doc GC GLP HPLC
  • January 28, 2020
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Checklist for Review of Analytical Raw Data (Chemical)

Checklist for review of analytical raw data generated during the chemical analysis of finished drug product, the raw material (API-Active.

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Audit GLP QC Sop Quality Control SOPs
  • January 22, 2020
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SOP for Audit Trail Review and Privilege Policy 

In the Quality Control Laboratory of the pharmaceutical product manufacturing unit, Different instruments, and equipment being used to analyze the.

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Audit cGMP QA Sop SOPs
  • December 28, 2019
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SOP for Vendor Management

The manufacturer or supplier who is supplying the material in routine and registered for the supply of specific material after.

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Audit cGMP Doc QA Sop SOPs
  • December 25, 2019
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Record Retention and Archival Policy

The retention period for the Documents and Records in which record shall be retained /preserved in a facility according to.

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Audit cGMP Checklist / Formats QA Sop SOPs
  • November 23, 2019
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Internal Audit (Self Inspection) Checklist

Internal Audit (Self Inspection) checklist for various departments of Pharmaceuticals like Quality Control, Quality Assurance, Production, HR and EHS etc..

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Audit cGMP QA Sop SOPs
  • November 21, 2019
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SOP on Internal Audit and Self Inspection

In the SOP on Internal Audit and Self Inspection, describe the detailed procedure to carryout the the Self inspection and.

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