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Author: Auditor

Capsule: SOP for Adjusting Gelatin Composition for Seasonal Variations – V 2.0

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Capsule: SOP for Adjusting Gelatin Composition for Seasonal Variations – V 2.0 Standard Operating Procedure for Adjusting Gelatin Composition for Seasonal Variations Department Capsule Manufacturing SOP No. SOP/CM/106/2025 Supersedes SOP/CM/106/2022 Page No. Page 1 of 6 Issue Date 01/02/2025 Effective Date 05/02/2025 Review Date 01/02/2026 1. Purpose The purpose of this SOP is to outline…

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Capsules V 2.0

SOP for Periodic Reorganization and Optimization of Warehouse Space – V 2.0

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SOP for Periodic Reorganization and Optimization of Warehouse Space – V 2.0 Standard Operating Procedure for Periodic Reorganization and Optimization of Warehouse Space Department Warehouse / Quality Assurance SOP No. SOP/RM/133/2025 Supersedes SOP/RM/133/2022 Page No. Page 1 of 15 Issue Date 28/02/2025 Effective Date 04/03/2025 Review Date 28/02/2026 1. Purpose This Standard Operating Procedure (SOP)…

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Raw Material Warehouse V 2.0

Capsule: SOP for Ensuring Compliance with GMP in Capsule Production – V 2.0

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Capsule: SOP for Ensuring Compliance with GMP in Capsule Production – V 2.0 Standard Operating Procedure for Ensuring Compliance with GMP in Capsule Production Department Capsule Manufacturing SOP No. SOP/CM/105/2025 Supersedes SOP/CM/105/2022 Page No. Page 1 of 6 Issue Date 01/02/2025 Effective Date 05/02/2025 Review Date 01/02/2026 1. Purpose The purpose of this SOP is…

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Capsules V 2.0

Creams: SOP for Homogenization in Cream Manufacturing – V 2.0

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Creams: SOP for Homogenization in Cream Manufacturing – V 2.0 Standard Operating Procedure for Homogenization in Cream Manufacturing Department Creams SOP No. SOP/CRM/044/2025 Supersedes SOP/CRM/044/2022 Page No. Page 1 of 6 Issue Date 03/10/2025 Effective Date 08/10/2025 Review Date 03/10/2026 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to outline the homogenization…

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Creams V 2.0

Ointments: SOP for Archiving Ointment Manufacturing Records – V 2.0

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SOP for Archiving Ointment Manufacturing Records – V 2.0 Procedure for Archiving Ointment Manufacturing Records Department Quality Assurance (QA)/Quality Control (QC)/Production SOP No. SOP/Ointment/160 Supersedes V 1.0 Page No. Page X of Y Issue Date [Insert Issue Date] Effective Date [Insert Effective Date] Review Date [Insert Review Date] 1. Purpose The purpose of this Standard…

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Ointments V 2.0

Tablets: SOP for Testing Thickness of Enteric Coating in Process – V 2.0

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Tablets: SOP for Testing Thickness of Enteric Coating in Process – V 2.0 Standard Operating Procedure for Testing Thickness of Enteric Coating in Process Department Tablet SOP No. SOP/TAB/160/2025 Supersedes SOP/TAB/160/2022 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 measuring and…

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Tablet Manufacturing V2.0

Capsule: SOP for Conducting Randomized Sampling of Capsules – V 2.0

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Capsule: SOP for Conducting Randomized Sampling of Capsules – V 2.0 Standard Operating Procedure for Conducting Randomized Sampling of Capsules Department Capsule Manufacturing SOP No. SOP/CM/104/2025 Supersedes SOP/CM/104/2022 Page No. Page 1 of 6 Issue Date 01/02/2025 Effective Date 05/02/2025 Review Date 01/02/2026 1. Purpose The purpose of this SOP is to establish a standardized…

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Capsules V 2.0

Aerosol: SOP for Compatibility Testing of Actuator and Formulation – V 2.0

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Aerosol: SOP for Compatibility Testing of Actuator and Formulation – V 2.0 SOP for Compatibility Testing of Actuator and Formulation Department Aerosol SOP No. SOP/Aerosol/067/2025 Supersedes SOP/Aerosol/067/2022 Page No. Page 1 of Y Issue Date 06/02/2025 Effective Date 16/02/2025 Review Date 06/02/2028 1. Purpose This Standard Operating Procedure (SOP) defines the process for conducting compatibility…

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Aerosols V 2.0

SOP for In-Process Quality Control Checks

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SOP for In-Process Quality Control Checks Comprehensive Guide to In-Process Quality Control Checks in Medical Device Manufacturing 1) Purpose The purpose of this SOP is to establish a systematic procedure for performing in-process quality control (IPQC) checks during the manufacturing of medical devices. These checks ensure that products meet specified standards and regulatory requirements at…

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Medical Devices

Capsule: SOP for Visual Inspection of Capsule Sealing – V 2.0

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Capsule: SOP for Visual Inspection of Capsule Sealing – V 2.0 Standard Operating Procedure for Visual Inspection of Capsule Sealing Department Capsule Manufacturing SOP No. SOP/CM/103/2025 Supersedes SOP/CM/103/2022 Page No. Page 1 of 6 Issue Date 01/02/2025 Effective Date 05/02/2025 Review Date 01/02/2026 1. Purpose The purpose of this SOP is to establish the procedure…

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Capsules V 2.0

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Standard Operating Procedures V 1.0

  • Aerosols
  • Analytical Method Development
  • Bioequivalence Bioavailability Study
  • Capsule Formulation
  • Clinical Studies
  • Creams
  • Data Integrity
  • Dental Dosage Forms
  • Drug Discovery
  • Environment, Health and Safety
  • Formulation Development
  • Gels
  • Good Distribution Practice
  • Good Warehousing Practices
  • In-Process Control
  • Injectables
  • Liquid Orals
  • Liposome and Emulsion Formulations
  • Lotions
  • Lyophilized Products
  • Maintenance Dept.
  • Medical Devices
  • Metered-Dose Inhaler
  • Microbiology Testing
  • Nanoparticle Formulation
  • Nasal Spray Formulations
  • Nebulizers
  • Ocular (Eye) Dosage Forms
  • Ointments
  • Otic (Ear) Dosage Forms
  • Pharmacovigilance
  • Powder & Granules
  • Purchase Departments
  • Quality Assurance
  • Quality Control
  • Raw Material Stores
  • Regulatory Affairs
  • Tablet Manufacturing
  • Rectal Dosage Forms
  • Transdermal Patches
  • Vaginal Dosage Forms
  • Validations and Qualifications

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NEW! Revised SOPs – V 2.0

  • Aerosols V 2.0
  • API Manufacturing V 2.0
  • BA-BE Studies V 2.0
  • Capsules V 2.0
  • Creams V 2.0
  • Ointments V 2.0
  • Raw Material Warehouse V 2.0
  • Tablet Manufacturing V2.0

New Publication: A must for All.

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