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

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 Glove Box

Posted on By

SOP for Glove Box

Standard Operating Procedure for Using Glove Box

1) Purpose

The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the glove box in the pharmaceutical manufacturing of otic dosage forms to ensure containment and protection of sensitive materials from external contaminants.

2) Scope

This SOP applies to all personnel involved in the operation and maintenance of glove boxes in the pharmaceutical manufacturing facility.

3) Responsibilities

Operators: Responsible for correctly operating the glove box as per this SOP.
Quality Control (QC) Personnel: Responsible for monitoring and verifying containment within the glove box.
Maintenance Personnel: Responsible for maintaining the glove box in proper working condition.

See also  SOP for Sterile Holding Tank

4) Procedure

4.1 Pre-operation Checks
4.1.1 Inspection
4.1.1.1 Inspect the glove box for cleanliness and integrity before use.
4.1.1.2 Check that gloves are intact and in good condition.
4.1.1.3 Verify that all necessary supplies (e.g., desiccants, cleaning materials) are available.

4.1.2 Preparation
4.1.2.1 Ensure that the materials to be handled inside the glove box are compatible with containment requirements.
4.1.2.2 Perform any necessary setup of equipment or tools inside the glove box.

/> 4.1.2.3 Set up and check the gas purification system (if applicable).

4.2 Operation
4.2.1 Entry and Exit
4.2.1.1 Put on appropriate PPE, including gloves, before entering the glove box.
4.2.1.2 Open the glove box door slowly and enter while maintaining containment.
4.2.1.3 Close the door carefully to maintain the integrity of the glove box environment.

See also  SOP for Cleaning Validation

4.2.2 Handling Procedures
4.2.2.1 Handle materials and equipment inside the glove box gently to avoid spills or contamination.
4.2.2.2 Use designated tools and equipment suitable for use inside the glove box.
4.2.2.3 Follow all procedures to prevent moisture ingress or exposure to outside contaminants.

4.3 Post-operation
4.3.1 Exit and Cleanup
4.3.1.1 Remove gloves and dispose of them properly as per facility protocols.
4.3.1.2 Perform any required cleaning of the glove box interior and replace desiccants as needed.
4.3.1.3 Leave the glove box in a clean and ready condition for the next use.

4.3.2 Maintenance
4.3.2.1 Regularly inspect gloves for wear and replace them as necessary.
4.3.2.2 Clean the glove box exterior and monitor seals and connections for leaks.
4.3.2.3 Perform scheduled maintenance and certification of gas purification systems (if applicable).

See also  SOP for Laboratory Refrigerator

5) Abbreviations, if any

QC: Quality Control
SOP: Standard Operating Procedure
PPE: Personal Protective Equipment

6) Documents, if any

Glove box log
Maintenance records for the glove box

7) Reference, if any

Manufacturer’s manual for the glove box
Pharmacopeial guidelines for containment systems in pharmaceutical manufacturing

8) SOP Version

Version 1.0

Otic (Ear) Dosage Forms Tags:Cleaning validation in otic manufacturing, Ear Drops dosage form SOP, Ear Drops SOP, EarDrops SOP, Environmental monitoring in otic manufacturing, GMP for Ear Drops, GMP for otic products, Otic dosage form calibration SOP, Otic dosage form equipment cleaning SOP, Otic dosage form quality assurance, Otic dosage form SOP, Otic drug complaint handling SOP, Otic drug documentation control SOP, Otic drug in-process control SOP, Otic drug stability testing SOP, Otic manufacturing process SOP, Otic product batch record SOP, Otic product deviation handling SOP, Otic product raw material handling SOP, Otic product self-inspection SOP, Otic product vendor qualification SOP, Otic solution SOP, Otic suspension SOP, Quality control for otic dosage forms, SOP for Ear Drops manufacturing, SOP for otic dosage form returned goods, SOP for otic dosage form training, SOP for otic drug manufacturing, SOP for otic formulation development, SOP for otic product labeling, SOP for otic product packaging, SOP for otic product recalls, SOP for otic product release, SOP for otic product sampling

Post navigation

Previous Post: SOP for Cryogenic Mill
Next Post: SOP for In-Process Checkweigher

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