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

In-Process Control: SOP for Leak Testing of Sealed Containers

Posted on By

SOP for Leak Testing of Sealed Containers

Procedure for Leak Testing of Sealed Containers

1) Purpose

The purpose of this SOP is to outline the procedure for conducting leak testing on sealed containers to ensure their integrity and prevent leakage of pharmaceutical products.

2) Scope

This SOP applies to all types of sealed containers (e.g., vials, ampoules, bottles) used for pharmaceutical products within the facility.

3) Responsibilities

Quality Control (QC) Department: Responsible for performing leak testing and ensuring compliance with this SOP.
Production Department: Responsible for providing sealed containers and supporting QC during testing.

4) Procedure

4.1 Equipment Preparation:
    4.1.1 Verify and calibrate the leak testing equipment (e.g., helium leak detector, bubble emission tester).
    4.1.2 Ensure all necessary accessories and consumables are available and in working condition.
    4.1.3 Perform equipment suitability checks according to validated procedures.

See also  SOP for Blister Pack Integrity Testing

4.2 Sample Selection:
    4.2.1 Select representative samples of sealed containers from different batches.
    4.2.2 Ensure samples cover various container sizes, closure types, and production dates.
    4.2.3 Handle samples carefully to avoid compromising their integrity.

4.3 Leak Testing Procedure:
    4.3.1 Perform leak testing using the selected method (e.g., helium leak detection, bubble emission).
    4.3.2 Apply the testing method according to the manufacturer’s instructions and validated procedures.
    4.3.3 Record testing parameters, including test conditions, leakage thresholds, and

results.

4.4 Interpretation of Results:
    4.4.1 Evaluate test results to identify any containers exhibiting leaks or breaches in integrity.
    4.4.2 Compare testing results against acceptance criteria specified in pharmacopeial standards or internal specifications.
    4.4.3 Document and investigate any deviations from expected results, including re-testing if necessary.

See also  SOP for Redispersibility Testing in Suspensions

4.5 Acceptance Criteria:
    4.5.1 Sealed containers are considered acceptable if they pass the leak test without exceeding specified leakage limits.
    4.5.2 Ensure all testing parameters and acceptance criteria meet predefined standards.

4.6 Documentation:
    4.6.1 Record all leak testing procedures, results, and observations in the Leak Testing Record.
    4.6.2 Maintain detailed records of equipment calibration, sample selection, testing conditions, and any deviations encountered.
    4.6.3 Review and approve the documentation by QC Manager.

5) Abbreviations, if any

QC: Quality Control

6) Documents, if any

Leak Testing Record
Equipment Calibration Certificates
Sampling Plan Document

7) Reference, if any

USP General Chapter <1207> – Package Integrity Evaluation
Pharmacopeial standards for Leak Testing of Sealed Containers

See also  SOP for Aseptic Process Simulation (Media Fill)

8) SOP Version

Version 1.0

In-Process Control Tags:Blend uniformity testing SOP, Bulk density testing SOP, Capsule content uniformity SOP, Capsule disintegration testing SOP, Capsule dissolution testing SOP, Capsule weight variation SOP, Clarity and opalescence testing of liquids SOP, Endotoxin testing in injectable products SOP, Flowability testing of powders SOP, Granulation size distribution SOP, Moisture content determination in granules SOP, Osmolality testing SOP, Particulate matter testing in liquids SOP, pH measurement of solutions SOP, Pyrogen testing SOP, Specific gravity testing of liquids SOP, Sterility testing SOP, Tablet disintegration testing SOP, Tablet dissolution testing SOP, Tablet friability testing SOP, Tablet hardness testing SOP, Tablet thickness measurement SOP, Tablet weight variation SOP, Uniformity of dosage units SOP, Viscosity testing of liquids SOP

Post navigation

Previous Post: SOP for Container Closure Integrity Testing
Next Post: In-Process Control: SOP for Visual Inspection of Injectable Products

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