SOP for In–Process Quality Control Records

Objective

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

Purpose

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

Scope

Procedure for In-process Quality control & Records.

Responsibility

Primary: Production chemist.

Secondary: Production Officer.

Procedure

• 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 the progress of the batch and after completion of the 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.

Abbreviation

SOP: Standard Operating Procedure 

QC: Quality Control

IPQC: In-process Quality Control

Annexure

Nil

Revision History

Nil

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