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Line clearance is a structured procedure for ensuring that the equipment and work area are free of products, documents and materials from the previous process that are not required for the next scheduled process, and that the equipment is clean and ready for the next scheduled process.
Line clearance is a standardized procedure in manufacturing for ensuring equipment and work areas are free of products, documents, and materials from a previous process. Line clearance procedures help operators prepare for the next scheduled process and avoid mislabeling or cross-contamination of finished products.
Line Clearance Checklist for Packing Line (Tablet & Capsule) Check and ensure that the area/ equipment/ belt are visually clean. Check the proper gowning of personnel. Check the present status label which shows the details. Ensure the availability of BPR and filled upto the stage.
IPQA of Dispensing, Manufacturing, Packaging and Dispatch activities. Review and Control of SOP's, Specification, BPR issuance, Master Formulae and Records. Preparation & Review of process validation protocols and reports. Executing the validation/revalidation activity in the absence of authorized person.
In pharmacology, clearance is a pharmacokinetic measurement of the volume of plasma from which a substance is completely removed per unit time. Usually, clearance is measured in L/h or mL/min. The quantity reflects the rate of drug elimination divided by plasma concentration.
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Line clearance is a standardized procedure in manufacturing for ensuring equipment and work areas are free of products, documents, and materials from a previous process. Line clearance procedures help operators prepare for the next scheduled process and avoid mislabeling or cross-contamination of finished products.
1. Type-A Area clearance : During batch change over of same product. 2. Type-B Area clearance : During batch change over of same product with different strength.
TYPE A: MINOR à This type of cleaning take place between two batches of same product or between different strengths of the same product. For minor cleaning, cleaning validation is not required, since cross contamination is not an issue. TYPE B: MAJOR à This type of cleaning take place between two products.

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