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In–Process Quality Control Records

Purpose: 
To provide a documented procedure for In–process Quality control Records.

Objective: 
To provide a guideline for In–process Quality control Records.

Scope: 
Procedure for In- process Quality control & Records.

Responsibility:
Primary: Production chemist.
Secondary: Production Officer.

Procedure:

Operation:
  • Start Batch as per BMR of the product to control the progress of reaction and follow In- process Quality control system norms and the procedure to be followed as under.
  • As per progress of the batch and after completion of mentioned time of the reaction, remove the sample and send to Q.C for analysis in cleaned bottle.
  • Fill the sample details of product name/ stage/ B. No./ reaction time and sampling equipment in specially designed form for IPQC test i.e. INPROCESS TEST information sheet Collect the result of IPQC sample with Document duly signed by Q.C. analysis.
  • Send the filled IPQC form to Q.C. department for immediate sample analysis.
  • Attach IPQC report with BMR and fill analysis report in BMR.

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