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SOP Guide for Pharma

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Author: Auditor

Tablets: SOP for Monitoring and Adjusting Spray Nozzles in Coating Machines – V 2.0

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Tablets: SOP for Monitoring and Adjusting Spray Nozzles in Coating Machines – V 2.0 Standard Operating Procedure for Monitoring and Adjusting Spray Nozzles in Coating Machines Department Tablet SOP No. SOP/TAB/169/2025 Supersedes SOP/TAB/169/2022 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…

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Tablet Manufacturing V2.0

Creams: SOP for In-Line Filtration of Creams before Packing – V 2.0

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Creams: SOP for In-Line Filtration of Creams before Packing – V 2.0 Standard Operating Procedure for In-Line Filtration of Creams before Packing Department Creams SOP No. SOP/CRM/051/2025 Supersedes SOP/CRM/051/2022 Page No. Page 1 of 6 Issue Date 07/11/2025 Effective Date 12/11/2025 Review Date 07/11/2026 1. Purpose The purpose of this Standard Operating Procedure (SOP) is…

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Creams V 2.0

SOP for Handling Raw Materials with Specific Toxicity or Carcinogenicity Risks – V 2.0

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SOP for Handling Raw Materials with Specific Toxicity or Carcinogenicity Risks – V 2.0 Standard Operating Procedure for Handling Raw Materials with Specific Toxicity or Carcinogenicity Risks Department Warehouse / Quality Assurance / Safety Department SOP No. SOP/RM/140/2025 Supersedes SOP/RM/140/2022 Page No. Page 1 of 15 Issue Date 09/03/2025 Effective Date 16/03/2025 Review Date 09/03/2026…

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Raw Material Warehouse V 2.0

Capsule: SOP for Cleaning Capsule Drying Trays and Racks – V 2.0

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Capsule: SOP for Cleaning Capsule Drying Trays and Racks – V 2.0 Standard Operating Procedure for Cleaning Capsule Drying Trays and Racks Department Capsule Manufacturing SOP No. SOP/CM/120/2025 Supersedes SOP/CM/120/2022 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…

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Capsules V 2.0

SOP for Final Quality Inspection of Medical Devices

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SOP for Final Quality Inspection of Medical Devices Comprehensive Guide to Final Quality Inspection of Medical Devices 1) Purpose The purpose of this SOP is to define a standardized procedure for conducting final quality inspections on medical devices before their release for distribution. This ensures that the devices meet the required quality, safety, and performance…

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Medical Devices

Ointments: SOP for Managing Retained Samples and Associated Records – V 2.0

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SOP for Managing Retained Samples and Associated Records – V 2.0 Procedure for Managing Retained Samples and Associated Records Department Quality Assurance (QA)/Quality Control (QC)/Warehouse SOP No. SOP/Ointment/168 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…

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Ointments V 2.0

Capsule: SOP for Cleaning Gelatin Feeders in Capsule Manufacturing – V 2.0

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Capsule: SOP for Cleaning Gelatin Feeders in Capsule Manufacturing – V 2.0 Standard Operating Procedure for Cleaning Gelatin Feeders in Capsule Manufacturing Department Capsule Manufacturing SOP No. SOP/CM/119/2025 Supersedes SOP/CM/119/2022 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 define…

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Capsules V 2.0

Tablets: SOP for Online Hardness Testing in Tablets During Compression – V 2.0

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Tablets: SOP for Online Hardness Testing in Tablets During Compression – V 2.0 Standard Operating Procedure for Online Hardness Testing in Tablets During Compression Department Tablet SOP No. SOP/TAB/168/2025 Supersedes SOP/TAB/168/2022 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 performing online…

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Tablet Manufacturing V2.0

Creams: SOP for Line Clearance in Manufacturing Areas – V 2.0

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Creams: SOP for Line Clearance in Manufacturing Areas – V 2.0 Standard Operating Procedure for Line Clearance in Manufacturing Areas Department Creams SOP No. SOP/CRM/050/2025 Supersedes SOP/CRM/050/2022 Page No. Page 1 of 7 Issue Date 02/11/2025 Effective Date 07/11/2025 Review Date 02/11/2026 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to define…

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Creams V 2.0

Capsule: SOP for Cleaning Hopper Bins for Capsule Filling Machines – V 2.0

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Capsule: SOP for Cleaning Hopper Bins for Capsule Filling Machines – V 2.0 Standard Operating Procedure for Cleaning Hopper Bins for Capsule Filling Machines Department Capsule Manufacturing SOP No. SOP/CM/118/2025 Supersedes SOP/CM/118/2022 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

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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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