Pharmaceutical Guidelines

Quality Assurance (QA) in the Pharmaceutical industry, is very essential for ensuring that Pharmaceutical Products are manufactured to a safe and consistent standard, and references with the guidelines, WHO, GMP are the main principles for pharmaceutical products.

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Sunday 6 December 2020

Return Of Goods SOP

 
To lay down the procedure for handling of ‘’Return of finish good’’.

RESPONSIBILITY:

FG store is responsible for receipt of return goods and intimate to Plant Head/QA HOD
Quality Assurance department responsible for investigating the goods and record the investigation report.
Plant Head/QA HOD responsible for taking action plain as per the investigation report and return goods procedure.  

ACCOUNTABILITY:

The accountability lies upon Quality Assurance Head & Plant Head for the implementation and complies of the SOP.

PROCEDURE: 
         
Finish good store receipt the returned goods it shall be stored in an area marked for “Returned Goods” in Bonded Store Room (BSR). And if the goods have been returned against recall it shall be stored in area marked as “Recalled Product”. If the goods have been returned due to Product Recall, then it shall be treated as per SOP No. SOP-QA-021.

In case of returned Goods, BSR Personnel shall fill the Returned Goods Log Format No. F/QA-021-01 with details like Sr. No., Date of return, Name of Party, Product Name, Batch No., Quantity received after reprocess, Dispatch Quantity and Invoice No.  Remarks if any.

The BSR Personnel shall then fill the Returned Goods Form Format No. F/QA-021-02 with Product details like Name, Batch No., Mfg. Date, Exp. Date, Returned by (Name) and address, Reason for return and send it to Quality Assurance as intimation.

The Quality Assurance Officer shall then go and investigate the goods and record the investigation report.

No Defect – Goods shall be returned to manufacturing.

Short Expiry or if the drug product does not meet the standard – Goods shall be destroyed as per SOP.

Goods are damaged in transit – Sample shall be sent for reanalysis and on receipt of the confirmatory report, goods shall be returned to manufacturing for repacking.

Final authorization for destruction or reprocessing shall be given by Quality Assurance HOD/Plant Head.
If the product is reprocessed then when it shall be dispatched and record maintained in the same.

LIST OF ANNEXURE AND FORMATS:    

Sr. No.

Title of Format

Format No.

01

Returned Goods Log

F/QA-021-01

02

Returned Goods Form

F/QA-021-02

 
 

 

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