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Tag: Capsule sealing methods

Capsule: SOP for Ensuring Traceability in Capsule Manufacturing Documentation – V 2.0

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Capsule: SOP for Ensuring Traceability in Capsule Manufacturing Documentation – V 2.0 Standard Operating Procedure for Ensuring Traceability in Capsule Manufacturing Documentation Department Quality Assurance SOP No. SOP/QA/225/2025 Supersedes SOP/QA/225/2022 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 ensure…

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Capsules V 2.0

Capsule: SOP for Maintaining Training Records for Capsule Operators – V 2.0

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Capsule: SOP for Maintaining Training Records for Capsule Operators – V 2.0 Standard Operating Procedure for Maintaining Training Records for Capsule Operators Department Human Resources / Production SOP No. SOP/HR/224/2025 Supersedes SOP/HR/224/2022 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

Capsule: SOP for Documenting QC Test Results for Capsules – V 2.0

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Capsule: SOP for Documenting QC Test Results for Capsules – V 2.0 Standard Operating Procedure for Documenting QC Test Results for Capsules Department Quality Control SOP No. SOP/QC/223/2025 Supersedes SOP/QC/223/2022 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

Capsule: SOP for Recordkeeping for Stability Studies of Capsules – V 2.0

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Capsule: SOP for Recordkeeping for Stability Studies of Capsules – V 2.0 Standard Operating Procedure for Recordkeeping for Stability Studies of Capsules Department Quality Control SOP No. SOP/QC/222/2025 Supersedes SOP/QC/222/2022 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

Capsule: SOP for Documentation of Process Deviations in Capsule Production – V 2.0

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Capsule: SOP for Documentation of Process Deviations in Capsule Production – V 2.0 Standard Operating Procedure for Documentation of Process Deviations in Capsule Production Department Production SOP No. SOP/PD/221/2025 Supersedes SOP/PD/221/2022 Page No. Page 1 of 5 Issue Date 01/02/2025 Effective Date 05/02/2025 Review Date 01/02/2026 1. Purpose The purpose of this SOP is to…

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Capsules V 2.0

Capsule: SOP for Maintaining Cleaning Logs for Capsule Equipment – V 2.0

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Capsule: SOP for Maintaining Cleaning Logs for Capsule Equipment – V 2.0 Standard Operating Procedure for Maintaining Cleaning Logs for Capsule Equipment Department Production SOP No. SOP/PD/220/2025 Supersedes SOP/PD/220/2022 Page No. Page 1 of 5 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 the…

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Capsules V 2.0

Capsule: SOP for Preparing Batch Packing Records for Capsules – V 2.0

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Capsule: SOP for Preparing Batch Packing Records for Capsules – V 2.0 Standard Operating Procedure for Preparing Batch Packing Records for Capsules Department Packaging SOP No. SOP/PKG/219/2025 Supersedes SOP/PKG/219/2022 Page No. Page 1 of 5 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 the…

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Capsules V 2.0

Capsule: SOP for Archiving Capsule Manufacturing Records – V 2.0

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Capsule: SOP for Archiving Capsule Manufacturing Records – V 2.0 Standard Operating Procedure for Archiving Capsule Manufacturing Records Department Quality Control SOP No. SOP/QC/218/2025 Supersedes SOP/QC/218/2022 Page No. Page 1 of 5 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 procedure for the…

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Capsules V 2.0

Capsule: SOP for Reviewing Batch Manufacturing Records (BMRs) – V 2.0

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Capsule: SOP for Reviewing Batch Manufacturing Records (BMRs) – V 2.0 Standard Operating Procedure for Reviewing Batch Manufacturing Records (BMRs) Department Quality Control SOP No. SOP/QC/217/2025 Supersedes SOP/QC/217/2022 Page No. Page 1 of 5 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 the procedure…

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Capsules V 2.0

Capsule: SOP for Preparing Batch Manufacturing Records for Capsules – V 2.0

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Capsule: SOP for Preparing Batch Manufacturing Records for Capsules – V 2.0 Standard Operating Procedure for Preparing Batch Manufacturing Records for Capsules Department Production SOP No. SOP/PD/216/2025 Supersedes SOP/PD/216/2022 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…

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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

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