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 Operating Lyophilizers for Nasal Powders

Posted on By




SOP for Operating Lyophilizers for Nasal Powders



Standard Operating Procedure for Operating Lyophilizers for Nasal Powders

1) Purpose

This SOP outlines the procedures for operating lyophilizers to produce nasal powder formulations. Lyophilization, or freeze-drying, ensures that moisture is removed from nasal powders, preserving the product’s stability and shelf life.

2) Scope

This SOP applies to all personnel involved in the operation and maintenance of lyophilizers used for nasal powder production at [Company Name].

3) Responsibilities

  • Operators: Responsible for setting up and operating the lyophilizer according to product specifications and batch requirements.
  • Quality Assurance (QA): Ensures that the lyophilized powders meet the required moisture content and stability specifications.
  • Maintenance Team: Ensures the lyophilizer is functional and calibrated for accurate temperature and vacuum control.

4) Procedure

4.1 Pre-Operation Setup

4.1.1 Inspection of Lyophilizer

  • Visually inspect the lyophilizer to ensure that it has been properly cleaned and is free of any residues from previous batches. Verify that all seals, gaskets, and connections are secure.
  • Document the pre-operation inspection in the equipment log.
See also  SOP for Incorporating Antioxidants in Nasal Spray Formulations

4.1.2 Setup Parameters

  • Set the lyophilizer parameters, including freezing temperature, primary drying temperature, secondary drying temperature, and vacuum level, according to the formulation’s requirements. Record the settings in the Batch Manufacturing Record (BMR).
  • Ensure that the product trays are correctly loaded and spaced for efficient heat transfer.

4.2 Operation of the Lyophilizer

4.2.1 Freeze-Drying Process

  • Start the freeze-drying cycle by freezing the product at the specified freezing temperature. Monitor the chamber temperature to ensure that the product is frozen uniformly.
  • Once the product is completely frozen, initiate the primary drying phase by reducing the chamber pressure to the required vacuum level and gradually raising the shelf temperature to sublimate the frozen water.
  • Continue the primary drying process until the majority of the water has been removed, then transition to the secondary drying phase to remove any remaining bound water.
See also  SOP for Employee Training and Competency Development

4.2.2 In-Process Checks

  • Perform regular checks on the product’s moisture content and temperature during the freeze-drying cycle. Record the moisture content in the in-process testing log.
  • Adjust the drying parameters if necessary to achieve the desired moisture content. Record any adjustments in the BMR.

4.3 Post-Operation Activities

4.3.1 Shutdown Procedure

  • After the freeze-drying cycle is complete, stop the vacuum and return the chamber to atmospheric pressure. Open the chamber and carefully remove the lyophilized product trays.
  • Turn off the lyophilizer and allow the unit to cool down before cleaning or performing maintenance.

4.3.2 Cleaning of Lyophilizer

  • Disassemble any removable parts and clean all components with an approved cleaning solution. Rinse thoroughly with sterile water and allow to air dry or use lint-free wipes.
  • Document the cleaning process in the cleaning log and submit for QA review before the next operation.
See also  SOP for Operation and Maintenance of HVAC Systems

4.4 Maintenance of Lyophilizer

4.4.1 Routine Maintenance

  • Inspect the lyophilizer weekly for wear and tear on critical components such as vacuum pumps and heat transfer plates. Perform any necessary repairs or replacements as needed.
  • Record all maintenance activities in the maintenance log.

4.4.2 Annual Calibration

  • Calibrate the lyophilizer’s temperature control and vacuum systems annually to ensure accurate freeze-drying performance. Document calibration results in the calibration log.

5) Abbreviations, if any

  • BMR: Batch Manufacturing Record
  • QA: Quality Assurance

6) Documents, if any

  • Batch Manufacturing Record (BMR)
  • In-Process Testing Log
  • Cleaning Log
  • Maintenance Log
  • Calibration Log

7) References, if any

  • Manufacturer’s lyophilizer manual
  • Internal SOP for cleaning and maintenance

8) SOP Version

Version 1.0

Annexure

1. In-Process Testing Log Template

Date Batch No. Moisture Content (%) Temperature (°C) Operator Initials QA Approval
DD/MM/YYYY Batch Number Moisture Content Measured Temperature Measured Operator Name QA Name
         


Nasal Spray Formulations Tags:Cleaning SOP for nasal spray equipment, Environmental control in nasal spray production, Equipment maintenance for nasal sprays, Formulating isotonic nasal sprays, Microbial stability in nasal formulations, Mixing SOP for nasal formulations, Nasal spray API formulation, Nasal spray batch manufacturing SOP, Nasal spray filling machine operation, Nasal spray formulation process, Nasal spray GMP guidelines, Nasal spray homogenization techniques, Nasal spray manufacturing process, Nasal spray packaging SOP, Nasal spray preservative-free formulation, Nasal spray production SOP, Nasal spray stability studies, Nasal spray sterilization process, Nasal spray viscosity monitoring, Particle size control in nasal sprays, pH adjustment in nasal formulations, Quality control in nasal spray production, Solvent selection for nasal sprays, SOP for nasal spray manufacturing, SOP for nasal spray testing

Post navigation

Previous Post: SOP for Optimizing Freeze-Drying Cycles
Next Post: Lyophilized Products : SOP for Primary Drying Process in Lyophilization

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