Standard Operating Procedure for Eye Drop Filling System in Ocular Dosage Form Manufacturing

1) Purpose

The purpose of this SOP is to establish a standardized procedure for the operation, cleaning, and maintenance of the eye drop filling system to ensure consistent, sterile, and accurate filling of ocular dosage forms.

2) Scope

This SOP applies to all eye drop filling systems used in the manufacturing of ocular dosage forms within the pharmaceutical manufacturing facility.

3) Responsibilities

Production personnel are responsible for operating the eye drop filling system and maintaining accurate records. Quality control personnel are responsible for verifying the filling process and ensuring compliance with SOPs.

4) Procedure

4.1 Preparation for Eye Drop Filling

1. Ensure the filling area is clean, organized, and free from contaminants.
2. Verify the availability and condition of all equipment, utensils, and materials needed for the filling process.
3. Calibrate the filling system according to the manufacturer’s instructions to ensure accurate fill volumes.
4. Record the batch number, product name, and quantity of eye drops to be filled in the batch production log.

4.2 Eye Drop Filling Process

1. Preparation of Filling Equipment
   1. Assemble the filling system components as per the manufacturer’s instructions.
   2. Sanitize all parts that come into contact with the eye drop solution using appropriate disinfectants.
   3. Set up the filling system with the required filling parameters (volume, speed, etc.).
2. Filling Operation
   1. Load the prepared eye drop solution into the hopper of the filling system.
   2. Start the filling system and begin filling the containers (bottles, vials, etc.) with the eye drop solution.
   3. Monitor the filling process to ensure accurate and consistent fill volumes.
   4. Perform in-process checks for fill weight/volume at regular intervals.
3. Sealing and Capping
   1. Once the containers are filled, proceed to seal or cap them according to the product specifications.
   2. Ensure that the sealing/capping equipment is properly set up and functioning.
   3. Inspect the sealed/capped containers for integrity and proper closure.
4. Quality Control Checks
   1. Take samples of the filled eye drop containers for quality control testing, including weight, fill volume, and sterility.
   2. Record the results of the quality control tests in the batch production log.
   3. If any parameters are out of specification, investigate and take corrective actions before proceeding.
5. Labeling and Packaging
   1. Label the filled and sealed containers with the batch number, product name, and other required information.
   2. Package the labeled containers according to the packaging SOP.
   3. Store the packaged containers in a designated area under controlled conditions.

4.3 Cleaning and Maintenance

1. Clean the eye drop filling system and all associated equipment thoroughly after each batch according to the cleaning SOP.
2. Inspect the system for any signs of wear or damage and perform necessary maintenance or repairs.
3. Record all cleaning and maintenance activities in the equipment logbook.

4.4 Documentation

1. Record the details of the eye drop filling process, including fill volumes, in-process checks, and quality control results, in the batch production log.
2. Ensure that all records are signed and dated by the personnel responsible for the filling.
3. Attach a copy of the batch production log to the batch production record for traceability.

4.5 Review and Approval

1. The quality assurance department should regularly review filling procedures and records to ensure compliance with SOPs and regulatory requirements.
2. Any discrepancies or deviations should be investigated, documented, and resolved promptly.
3. Review and update the SOP as necessary to reflect any changes in procedures, regulations, or industry standards.

5) Abbreviations, if any

SOP: Standard Operating Procedure

CAPA: Corrective and Preventive Actions

6) Documents, if any

1. Batch production log
2. Batch production record
3. Equipment logbook

7) Reference, if any

GMP Guidelines for Pharmaceutical Manufacturing

8) SOP Version

Version 1.0