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
  • 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)
  • SOP – Blog Post
  • Toggle search form

SOP for Water for Injection (WFI) Generation

Posted on By

SOP for Water for Injection (WFI) Generation

Standard Operating Procedure for Water for Injection (WFI) Generation

1) Purpose

The purpose of this SOP is to establish procedures for the generation of Water for Injection (WFI) to ensure it meets quality standards for use in the manufacturing process.

2) Scope

This SOP applies to all personnel involved in the generation of WFI at [Company Name] for the production of intramuscular, subcutaneous, and intravenous injection products.

3) Responsibilities

The responsibilities of this SOP include:
– Engineering Department: Operating and maintaining WFI generation equipment.
– Quality Assurance (QA) Department: Monitoring and approving WFI quality.

See also  SOP for Stability Testing of IM and SC Products

4) Procedure

4.1 Preparation for WFI Generation
4.1.1 Ensure the WFI generation system is clean and free from contaminants.
4.1.2 Verify that all system components are functioning properly.
4.2 WFI Generation Process
4.2.1 Start the WFI generation system according to the manufacturer’s instructions.
4.2.2 Monitor the system parameters such as temperature, pressure, and flow rate during operation.
4.2.3 Collect samples at specified intervals to test for quality parameters such as endotoxins, conductivity, and microbial contamination.
4.3 Quality Control and Monitoring
4.3.1 Conduct regular tests on WFI samples to ensure compliance with quality standards.
4.3.2 Record all test results and monitor trends over time to detect any deviations or issues.
4.4 Maintenance and Calibration
4.4.1 Perform regular maintenance on the WFI generation system as per the manufacturer’s guidelines.
4.4.2 Calibrate all measurement instruments regularly to ensure accuracy.
4.5 Documentation
4.5.1 Maintain records of all operations, tests, maintenance, and calibrations related to WFI generation.
4.5.2 Ensure all documentation is signed and dated by the responsible personnel.

See also  SOP for CAPA (Corrective and Preventive Actions) Management

5) Abbreviations, if any

– QA: Quality Assurance
– WFI: Water for Injection

6) Documents, if any

– WFI Generation Logs
– Quality Control Test Records
– Maintenance and Calibration Logs

7) Reference, if any

– Good Manufacturing Practices (GMP) Guidelines
– International Organization for Standardization (ISO) Standards

8) SOP Version

Version 1.0

Injectables Tags:Analytical method validation for injections, Aseptic media fill trials SOP, Bioburden testing for injections, Cleaning validation for injection equipment, Emulsion stability testing for injections, Formulation development for injections, Homogeneity testing for injections, IM injection SOP, Injection filling volume accuracy, Injection stability testing, Intramuscular injection procedure, Intravenous injection guidelines, IV injection SOP, Needle assembly for syringes SOP, Packaging integrity testing for injections, Particle size analysis for injections, Pre-filled syringe stability testing, Product sterility in aseptic processing, Reconstitution testing for injections, SC injection SOP, Subcutaneous injection technique, Syringe filling and capping SOP, Syringe labeling and inspection SOP, Temperature mapping in storage areas, Viscosity testing for injections

Post navigation

Previous Post: SOP for Humidity Mapping of Storage Areas
Next Post: SOP for Light Exposure Testing

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
  • 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

Go to mobile version