Skip to content
  • Clinical Studies
  • Schedule M
  • Stability Studies
  • Pharma GMP
  • Pharma Tips
  • Pharma Books
  • Pharma Validation
  • Pharma Regulatory

SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

  • Home
  • SOP Guidelines
    • SOP Development
    • SOP Training
    • SOP Compliance Monitoring
    • SOP Revision Processes
    • Pharmaceutical SOP templates
    • GMP documentation SOP
    • Data integrity SOP pharma
    • Manufacturing SOP pharmaceutical
    • FDA SOP guidance
    • eQMS SOP workflows
  • Job Safety Analysis (JSA)
    • Oral Dosage Forms (Tablets & Capsules)
    • Oral Liquid Dosage Forms (Syrups, Elixirs, Suspensions, Emulsions)
    • Powder and Granule Dosage Forms
    • Topical Dosage Forms (Creams, Ointments, Gels, Lotions, Pastes)
    • Transdermal Dosage Forms (Patches)
  • Standard Test Procedures (STP)
  • GMP Audit Findings
    • Non-Compliance
      • SOP Absence
      • Revision Control
      • Non-Adherence
      • Poor Writing
      • Training Failure
      • Data Integrity Gaps
      • Mismatch Between SOPs and Practice
      • Critical Operations
      • Regulatory Change
      • Emergency Changes
      • Third-Party SOPs
      • Inspection Readiness
      • Deviation Handling
      • CAPA Integration
      • Validation Alignment
      • System Integration
      • Uncontrolled Distribution
      • SOP Implementation Gaps
      • SOP Alignment with Validation
      • Change Control Linkage
  • Toggle search form

SOPs for Capsules V 2.0

Capsule: SOP for Daily and Weekly Cleaning of Capsule Manufacturing Tools – V 2.0

Posted on By

The purpose of this SOP is to provide clear guidelines for the daily and weekly cleaning of capsule manufacturing tools. This process ensures that all tools are cleaned adequately after use to prevent contamination, cross-contamination, and maintain product integrity. It also ensures compliance with Good Manufacturing Practices (GMP).

Click to read the full article.

Capsules V 2.0

Capsule: SOP for Cleaning Sampling Probes Used in Capsule Manufacturing – V 2.0

Posted on By

The purpose of this SOP is to provide a standardized method for cleaning sampling probes used in capsule manufacturing. These probes are critical for ensuring that product samples are free from contamination and meet quality specifications. The SOP ensures that sampling probes are cleaned thoroughly between uses to maintain the integrity of the manufacturing process and prevent cross-contamination.

Click to read the full article.

Capsules V 2.0

Capsule: SOP for Cleaning Stainless Steel Surfaces in Capsule Manufacturing Areas – V 2.0

Posted on By

The purpose of this SOP is to outline the process for cleaning stainless steel surfaces in capsule manufacturing areas. Proper cleaning is necessary to prevent contamination and maintain compliance with Good Manufacturing Practices (GMP). The cleaning procedures are designed to ensure that stainless steel surfaces are free from residues, product build-up, or microbial contamination.

Click to read the full article.

Capsules V 2.0

Capsule: SOP for Cleaning Equipment Between Soft Gel and Hard Gelatin Batches – V 2.0

Posted on By

The purpose of this SOP is to provide a standardized cleaning procedure for the equipment used in the production of soft gelatin and hard gelatin capsules. Cleaning is essential to avoid cross-contamination between different types of gelatin and ensure the quality and safety of the final product. This SOP ensures that all equipment is thoroughly cleaned before switching between soft and hard gelatin batches.

Click to read the full article.

Capsules V 2.0

Capsule: SOP for Cleaning Capsule Size Sorting Machines – V 2.0

Posted on By

The purpose of this SOP is to outline the cleaning procedure for capsule size sorting machines used in capsule manufacturing. Proper cleaning is necessary to maintain the efficiency and accuracy of the size sorting process and to prevent contamination between batches of capsules with different sizes or types. This SOP ensures that the sorting machines are cleaned thoroughly after each production run.

Click to read the full article.

Capsules V 2.0

Capsule: SOP for Cleaning Blender Machines Used in Capsule Production – V 2.0

Posted on By

The purpose of this SOP is to ensure that blender machines used in the production of capsule formulations are cleaned thoroughly between batches. Effective cleaning is essential to prevent cross-contamination between different capsule formulations and to maintain product quality. This SOP outlines the cleaning process to ensure that blender machines are free from residues, dust, and contaminants before the next production run.

Click to read the full article.

Capsules V 2.0

Capsule: SOP for Disposal of Cleaning Residues from Capsule Machines – V 2.0

Posted on By

The purpose of this SOP is to define the process for the proper disposal of cleaning residues from capsule manufacturing machines. Proper disposal of residues is critical to avoid contamination, ensure environmental compliance, and maintain workplace safety. This SOP ensures that all residues from cleaning operations, including dust, powders, cleaning agents, and other by-products, are disposed of in accordance with regulatory and safety guidelines.

Click to read the full article.

Capsules V 2.0

Capsule: SOP for Cleaning of Encapsulation Machine Sensors – V 2.0

Posted on By

The purpose of this SOP is to ensure the effective cleaning of sensors used in encapsulation machines. These sensors play a crucial role in the accurate operation of capsule filling machines, and proper cleaning is necessary to avoid inaccuracies caused by dust or product residues. This SOP provides a step-by-step process for cleaning sensors to ensure their optimal performance and longevity.

Click to read the full article.

Capsules V 2.0

Capsule: SOP for Routine Cleaning of Airlocks in Capsule Manufacturing Areas – V 2.0

Posted on By

The purpose of this SOP is to outline the routine cleaning procedure for airlocks in capsule manufacturing areas. Airlocks are critical to maintaining the cleanroom environment by preventing contamination between different areas. Proper cleaning of these airlocks ensures compliance with GMP, reduces the risk of cross-contamination, and maintains product quality.

Click to read the full article.

Capsules V 2.0

Capsule: SOP for Cleaning Dust Collection Systems in Capsule Production – V 2.0

Posted on By

The purpose of this SOP is to define the procedure for cleaning dust collection systems used in capsule production. These systems are essential for maintaining air quality by capturing dust and particles generated during capsule manufacturing. Regular cleaning ensures the system functions efficiently, prevents cross-contamination, and maintains a safe and clean manufacturing environment.

Click to read the full article.

Capsules V 2.0

Posts pagination

Previous 1 … 13 14 15 … 23 Next

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

Read SOPs in your Language:

 - 
Bengali
 - 
bn
English
 - 
en
Gujarati
 - 
gu
Hindi
 - 
hi
Malayalam
 - 
ml
Marathi
 - 
mr
Punjabi
 - 
pa
Tamil
 - 
ta
Telugu
 - 
te

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.

Copyright © 2025 SOP Guide for Pharma.

Powered by PressBook WordPress theme