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

Injectables: SOP for Gowning Procedures in Cleanroom Environment

Posted on By

SOP for Gowning Procedures in Cleanroom Environment

Standard Operating Procedure for Gowning Procedures in Cleanroom Environment

1) Purpose

The purpose of this SOP is to define the procedures for gowning in a cleanroom environment to prevent contamination of pharmaceutical products and ensure compliance with cleanliness standards.

2) Scope

This SOP applies to all personnel entering cleanrooms within the pharmaceutical manufacturing facility.

3) Responsibilities

3.1 Cleanroom Personnel

  • Follow gowning procedures accurately and consistently.
  • Report any deviations or issues related to gowning to supervisors.

3.2 Cleanroom Supervisor

  • Monitor gowning practices and ensure compliance with gowning SOP.
  • Provide training and guidance to personnel on gowning procedures.
See also  Injectables: SOP for Control of Non-Conforming Materials

4) Procedure

4.1 Gowning Sequence

  1. Perform hand hygiene according to handwashing protocols.
  2. Don cleanroom garments in the designated gowning area.

4.2 Gowning Steps

  1. Wear hair covers, beard covers (if applicable), and face masks as required.
  2. Put on cleanroom coveralls or gowns following proper technique.
  3. Don gloves and ensure proper fit and coverage.

4.3 Cleanroom Entry

  1. Proceed to the designated entry point of the cleanroom.
  2. Perform final visual inspection of gowning attire to ensure integrity.

4.4 Exiting the Cleanroom

  1. Remove gloves and dispose of them in designated waste containers.
  2. Remove gown and other PPE items in the designated doffing area.

5) Abbreviations, if any

SOP: Standard Operating Procedure

See also  Injectables: SOP for Document Control and Management

6) Documents, if any

  • Gowning SOP Training Records
  • Cleanroom Gowning Log
  • Procedure for Cleanroom Gowning

7) Reference, if any

ISO 14644-5: Cleanrooms and associated

controlled environments – Part 5: Operations
USP General Chapter <797>: Pharmaceutical Compounding – Sterile Preparations

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 Foreign Particulate Matter Testing in Gels
Next Post: SOP for Sterility Testing in Aseptic Gels

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