To lay down a procedure for finished product inspection and release.
This procedure is applicable for all type of finished pharmaceutical product.
Quality assurance, Warehouse and Production.
4.1 Physical inspection of finished goods:
4.1.1 Check the quarantine label has been attached on each pallet/shipper.
4.1.2 Check that the information on the quarantine label is correct.
4.1.3 Select the shipper randomly as per below sampling plan:
|Shipper checking policy|
|Sr. No.||Total No. of shipper in the batch||Number of shippers to be checked||Sr. No.||Total No. of shipper in the batch||Number of shippers to be checked|
|Inner carton checking policy|
|Sr. No.||Total number of inner cartons per shipper||Number of inner cartons to be checked|
4.1.4 Check the below parameters and record in inspection report.
Shippers: Correctness of seal, number of inner cartons, correctness of quarantine tag.
Inner carton: Legibility of batch details, appearance of inner carton
Leaflet: Availability of leaflet in inner carton, legibility of leaflet
Blister/strip/other: Quantity of blister/strip, Embossing/printing details
Label/Sticker: Adherence, correctness of batch details
Cap sealing: Intactness of sealing, correctness of batch details if any
Dispensing device: Availability of dropper, applicator etc if any
4.1.5 Reseal the shipper after inspection and sign on it.
4.1.6 Keep the inspection report with the batch document.
4.1.7 Sign in the quarantine label.
4.1.8 Ensure that the retention samples have been collected.
4.1.9 Send the batch documents to QA batch release team.
4.2 Batch document review and finished product release:
4.2.1 Review the batch document and ensure that the required informations are available.
4.2.2 Review that all the required information filled and meets acceptance criteria.
4.2.3 Review that calculations are done correctly.
4.2.4 Ensure signatures are present of concern personnel/operator wherever applicable.
4.2.5 Review all steps are followed as per recommended procedure.
4.2.6 Ensure all necessary samples are collected and mentioned properly.
4.2.7 Review the correctness of reconciliation at each step.
4.2.8 Put the signature of “released by QA” on batch document.
4.2.9 Issue batch release certificate and attach with batch document.
4.2.10 Issue a copy of batch release certificate to warehouse and affix the release label on shippers/pellets.
4.2.11 Release the stock either in electronic system or intimate the warehouse by release note.
Copyright Notice: This Article/SOP/Compilation/Published Content is protected by Indian & International Copyright Laws. Reproduction and Distribution of the same without written permission is prohibited. Mail us at: firstname.lastname@example.org
For any Feedback or suggestion mail at: email@example.com
Weblink – https://pharmastate.com/