Tag: Tablet disintegration test procedure

Tablets: SOP for Screening and Milling of Granules for Tablets – V 2.0

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Tablets: SOP for Screening and Milling of Granules for Tablets – V 2.0 Standard Operating Procedure for Screening and Milling of Granules for Tablets Department Tablet SOP No. SOP/TAB/005/2025 Supersedes SOP/TAB/005/2022 Page No. Page 1 of 8 Issue Date 05/03/2025 Effective Date 10/03/2025 Review Date 05/03/2026 1. Purpose To outline the procedure for screening and…

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Tablet Manufacturing V2.0

Tablets: SOP for Binder Preparation for Granulation Process – V 2.0

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Tablets: SOP for Binder Preparation for Granulation Process – V 2.0 Standard Operating Procedure for Binder Preparation for Granulation Process Department Tablet SOP No. SOP/TAB/004/2025 Supersedes SOP/TAB/004/2022 Page No. Page 1 of 8 Issue Date 01/03/2025 Effective Date 05/03/2025 Review Date 01/03/2026 1. Purpose The purpose of this SOP is to define the process for…

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Tablet Manufacturing V2.0

Tablets: SOP for Dry Granulation Method for Tablets – V 2.0

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Tablets: SOP for Dry Granulation Method for Tablets – V 2.0 Standard Operating Procedure for Dry Granulation Method for Tablets Department Tablet SOP No. SOP/TAB/003/2025 Supersedes SOP/TAB/003/2022 Page No. Page 1 of 10 Issue Date 25/02/2025 Effective Date 01/03/2025 Review Date 25/02/2026 1. Purpose To define the procedure for the dry granulation method in tablet…

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Tablet Manufacturing V2.0

Tablets: SOP for Wet Granulation Equipment Setup and Operation – V 2.0

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Tablets: SOP for Wet Granulation Equipment Setup and Operation – V 2.0 Standard Operating Procedure for Wet Granulation Equipment Setup and Operation Department Tablet SOP No. SOP/TAB/002/2025 Supersedes SOP/TAB/002/2022 Page No. Page 1 of 10 Issue Date 20/02/2025 Effective Date 25/02/2025 Review Date 20/02/2026 1. Purpose To establish a standardized, GMP-compliant method for setting up…

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Tablet Manufacturing V2.0

Tablets: SOP for Granulation Process for Immediate Release Tablets – V 2.0

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Tablets: SOP for Granulation Process for Immediate Release Tablets – V 2.0 Standard Operating Procedure for Granulation Process for Immediate Release Tablets Department Tablet SOP No. SOP/TAB/001/2025 Supersedes SOP/TAB/001/2022 Page No. Page 1 of 10 Issue Date 15/02/2025 Effective Date 20/02/2025 Review Date 15/02/2026 1. Purpose To establish the granulation process for immediate release tablets,…

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Tablet Manufacturing V2.0

SOP for Batch Sampling and Testing

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Standard Operating Procedure for Batch Sampling and Testing 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for the systematic and controlled sampling and testing of batches in the pharmaceutical manufacturing process. This SOP ensures that representative samples are collected and tested for quality attributes, ensuring that the batch meets…

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Quality Control, Tablet Manufacturing

Tablet Manufacturing: SOP for Batch Record Review and Approval

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Standard Operating Procedure for Batch Record Review and Approval 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for the systematic and thorough review and approval of batch records in the pharmaceutical manufacturing facility. This SOP ensures that each batch record is meticulously examined for accuracy, completeness, and compliance with…

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Tablet Manufacturing

SOP for Batch Release and Product Release

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Standard Operating Procedure for Batch Release and Product Release 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for the systematic and controlled process of batch release and product release in the pharmaceutical manufacturing facility. This SOP ensures that each batch of pharmaceutical products undergoes thorough review, testing, and verification…

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Tablet Manufacturing

SOP for Batch Record Preparation and Documentation

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Standard Operating Procedure for Batch Record Preparation and Documentation 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for the proper preparation and documentation of batch records in the pharmaceutical manufacturing process. This SOP ensures that batch records are accurately and comprehensively documented, reflecting all critical steps, measurements, and observations…

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Tablet Manufacturing

SOP for Equipment Verification and Calibration

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Standard Operating Procedure for Equipment Verification and Calibration 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for the verification and calibration of equipment used in the pharmaceutical manufacturing process. This SOP ensures that all equipment is regularly checked for accuracy, precision, and compliance with required specifications to maintain the…

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Quality Assurance, Tablet Manufacturing