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.

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.

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.

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

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