Tag: Tablet disintegration test procedure

Tablets: SOP for Ensuring Compliance with FDA Guidelines – V 2.0 Standard Operating Procedure for Ensuring Compliance with FDA Guidelines Department Tablet SOP No. SOP/TAB/209/2025 Supersedes SOP/TAB/209/2022 Page No. Page 1 of 6 Issue Date 01/03/2026 Effective Date 06/03/2026 Review Date 01/03/2027 1. Purpose This SOP outlines the procedure for ensuring compliance with the FDA…

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Tablets: SOP for Approving Equipment Cleaning Procedures – V 2.0 Standard Operating Procedure for Approving Equipment Cleaning Procedures Department Tablet SOP No. SOP/TAB/208/2025 Supersedes SOP/TAB/208/2022 Page No. Page 1 of 6 Issue Date 01/03/2026 Effective Date 06/03/2026 Review Date 01/03/2027 1. Purpose The purpose of this SOP is to outline the procedure for approving equipment…

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Tablets: SOP for QA Oversight During Process Validation Studies – V 2.0 Standard Operating Procedure for QA Oversight During Process Validation Studies Department Tablet SOP No. SOP/TAB/207/2025 Supersedes SOP/TAB/207/2022 Page No. Page 1 of 7 Issue Date 01/03/2026 Effective Date 06/03/2026 Review Date 01/03/2027 1. Purpose This SOP outlines the process by which the QA…

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Tablets: SOP for Documentation of Stability Study Results – V 2.0 Standard Operating Procedure for Documentation of Stability Study Results Department Tablet SOP No. SOP/TAB/206/2025 Supersedes SOP/TAB/206/2022 Page No. Page 1 of 7 Issue Date 01/03/2026 Effective Date 06/03/2026 Review Date 01/03/2027 1. Purpose This SOP defines the procedure for documenting stability study results in…

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Tablets: SOP for Reviewing Cleaning Validation Protocols – V 2.0 Standard Operating Procedure for Reviewing Cleaning Validation Protocols Department Tablet SOP No. SOP/TAB/205/2025 Supersedes SOP/TAB/205/2022 Page No. Page 1 of 6 Issue Date 01/03/2026 Effective Date 06/03/2026 Review Date 01/03/2027 1. Purpose To define the procedure for reviewing cleaning validation protocols to ensure that all…

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Tablets: SOP for Validating Analytical Methods in QA – V 2.0 Standard Operating Procedure for Validating Analytical Methods in QA Department Tablet SOP No. SOP/TAB/204/2025 Supersedes SOP/TAB/204/2022 Page No. Page 1 of 7 Issue Date 01/03/2026 Effective Date 06/03/2026 Review Date 01/03/2027 1. Purpose To define the procedure for validating analytical methods used in quality…

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Tablets: SOP for Final Inspection of Coated Tablets Before Packing – V 2.0 Standard Operating Procedure for Final Inspection of Coated Tablets Before Packing Department Tablet SOP No. SOP/TAB/203/2025 Supersedes SOP/TAB/203/2022 Page No. Page 1 of 6 Issue Date 01/03/2026 Effective Date 06/03/2026 Review Date 01/03/2027 1. Purpose This SOP outlines the procedure for conducting…

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Tablets: SOP for Reviewing In-Process Quality Control Results – V 2.0 Standard Operating Procedure for Reviewing In-Process Quality Control Results Department Tablet SOP No. SOP/TAB/202/2025 Supersedes SOP/TAB/202/2022 Page No. Page 1 of 6 Issue Date 01/03/2026 Effective Date 06/03/2026 Review Date 01/03/2027 1. Purpose To establish the procedure for reviewing in-process quality control (IPQC) results…

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Tablets: SOP for Training Record Maintenance in QA Departments – V 2.0 Standard Operating Procedure for Training Record Maintenance in QA Departments Department Tablet SOP No. SOP/TAB/201/2025 Supersedes SOP/TAB/201/2022 Page No. Page 1 of 6 Issue Date 01/03/2026 Effective Date 06/03/2026 Review Date 01/03/2027 1. Purpose To define the procedure for maintaining training records for…

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Tablets: SOP for Preventive Action Reports (PAR) for Deviations – V 2.0 Standard Operating Procedure for Preventive Action Reports (PAR) for Deviations Department Tablet SOP No. SOP/TAB/200/2025 Supersedes SOP/TAB/200/2022 Page No. Page 1 of 6 Issue Date 01/03/2026 Effective Date 06/03/2026 Review Date 01/03/2027 1. Purpose To establish the procedure for the identification, documentation, and…

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