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SOP Guide for Pharma

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Tag: Capsule Manufacturing

Capsule: SOP for Handling APIs During Dispensing – V 2.0

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Capsule: SOP for Handling APIs During Dispensing – V 2.0 Standard Operating Procedure for Handling APIs During Dispensing Department Capsule Manufacturing SOP No. SOP/CM/004/2025 Supersedes SOP/CM/004/2022 Page No. Page 1 of 8 Issue Date 01/02/2025 Effective Date 05/02/2025 Review Date 01/02/2026 1. Purpose To define the procedure for handling Active Pharmaceutical Ingredients (APIs) during dispensing…

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Capsules V 2.0

Capsule: SOP for Labeling and Storage of Dispensed Materials – V 2.0

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Capsule: SOP for Labeling and Storage of Dispensed Materials – V 2.0 Standard Operating Procedure for Labeling and Storage of Dispensed Materials Department Capsule Manufacturing SOP No. SOP/CM/003/2025 Supersedes SOP/CM/003/2022 Page No. Page 1 of 8 Issue Date 01/02/2025 Effective Date 05/02/2025 Review Date 01/02/2026 1. Purpose To define the procedure for the correct labeling…

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Capsules V 2.0

Capsule: SOP for Sampling Raw Materials for Quality Testing – V 2.0

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Capsule: SOP for Sampling Raw Materials for Quality Testing – V 2.0 Standard Operating Procedure for Sampling Raw Materials for Quality Testing Department Capsule Manufacturing SOP No. SOP/CM/002/2025 Supersedes SOP/CM/002/2022 Page No. Page 1 of 8 Issue Date 01/02/2025 Effective Date 05/02/2025 Review Date 01/02/2026 1. Purpose To define the procedure for sampling raw materials…

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Capsules V 2.0

Capsule: SOP for Receiving Raw Materials for Capsule Manufacturing – V 2.0

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Capsule: SOP for Receiving Raw Materials for Capsule Manufacturing – V 2.0 Standard Operating Procedure for Receiving Raw Materials for Capsule Manufacturing Department Capsule Manufacturing SOP No. SOP/CM/001/2025 Supersedes SOP/CM/001/2022 Page No. Page 1 of 10 Issue Date 01/02/2025 Effective Date 05/02/2025 Review Date 01/02/2026 1. Purpose To define the procedure for receiving raw materials…

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Capsules V 2.0

SOP for Calibration and Maintenance: Procedures for Calibrating and Maintaining Equipment

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SOP for Calibration and Maintenance: Procedures for Calibrating and Maintaining Equipment Calibration and Maintenance Procedures 1) Purpose The purpose of this SOP is to establish standardized procedures for calibrating and maintaining equipment to ensure accurate and reliable performance. 2) Scope This SOP applies to all equipment used in the pharmaceutical manufacturing facility that requires calibration…

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Capsule Formulation

SOP for Document Control: Procedures for Managing the Creation, Approval, Distribution, and Archiving of Documents

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SOP for Document Control: Procedures for Managing the Creation, Approval, Distribution, and Archiving of Documents Document Control Procedures 1) Purpose The purpose of this SOP is to establish standardized procedures for managing the creation, approval, distribution, and archiving of documents to ensure accurate and up-to-date documentation within the pharmaceutical manufacturing facility. 2) Scope This SOP…

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Capsule Formulation

SOP for Cleaning and Sanitation: Procedures for Cleaning and Sanitizing Equipment and Facilities

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SOP for Cleaning and Sanitation: Procedures for Cleaning and Sanitizing Equipment and Facilities Cleaning and Sanitation Procedures 1) Purpose The purpose of this SOP is to establish standardized procedures for cleaning and sanitizing equipment and facilities to ensure a hygienic manufacturing environment and prevent contamination. 2) Scope This SOP applies to all equipment and facilities…

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Capsule Formulation

SOP for Change Control: Procedures for Managing Changes to Processes, Equipment, or Procedures

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SOP for Change Control: Procedures for Managing Changes to Processes, Equipment, or Procedures Change Control Procedures 1) Purpose The purpose of this SOP is to establish standardized procedures for managing changes to processes, equipment, or procedures to ensure that all changes are properly evaluated, documented, and implemented without negatively impacting product quality. 2) Scope This…

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Capsule Formulation

SOP for Employee Training: Procedures for Training Employees on Manufacturing Processes, Safety Protocols, and Quality Standards

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SOP for Employee Training: Procedures for Training Employees on Manufacturing Processes, Safety Protocols, and Quality Standards Employee Training Procedures 1) Purpose The purpose of this SOP is to establish standardized procedures for training employees on manufacturing processes, safety protocols, and quality standards to ensure competence and compliance. 2) Scope This SOP applies to all employees…

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Capsule Formulation

SOP for Auditing Suppliers: Procedures for Auditing and Qualifying Suppliers of Raw Materials and Components

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SOP for Auditing Suppliers: Procedures for Auditing and Qualifying Suppliers of Raw Materials and Components Supplier Auditing and Qualification Procedures 1) Purpose The purpose of this SOP is to establish standardized procedures for auditing and qualifying suppliers of raw materials and components to ensure they meet specified quality standards and regulatory requirements. 2) Scope This…

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Capsule Formulation

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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
  • Analytical Method Development V 2.0
  • API Manufacturing V 2.0
  • BA-BE Studies V 2.0
  • Biosimilars V 2.0
  • Capsules V 2.0
  • Creams V 2.0
  • Elixers V 2.0
  • Gels V 2.0
  • Injectables 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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