SOP for Eye Drop Filling Machine

SOP for Eye Drop Filling Machine

Standard Operating Procedure for Eye Drop Filling System

1) Purpose

The purpose of this SOP is to provide a detailed procedure for the operation and maintenance of the Eye Drop Filling Machine used in the manufacturing of ocular dosage forms.

2) Scope

This SOP applies to the Eye Drop Filling Machine used in the production of sterile eye drop solutions within the pharmaceutical manufacturing facility.

3) Responsibilities

The responsibilities include the operation, cleaning, and maintenance of the Eye Drop Filling Machine. The machine operator is responsible for following the procedure, and the maintenance team is responsible for regular maintenance and calibration.

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4) Procedure

4.1 Preparation

  1. Ensure the machine and surrounding area are clean and sanitized.
  2. Verify that the necessary components and consumables (bottles, caps, eye drop solution) are available and within expiry dates.
  3. Check that the machine is connected to the appropriate power supply.

4.2 Operation

  1. Turn on the machine and allow it to perform its self-checks.
  2. Load the bottles into the feeding system.
  3. Set the desired fill volume on the machine control panel.
  4. Initiate the filling process by pressing the start button.
  5. Monitor the filling process to ensure no overfilling or underfilling occurs.
  6. Once filling is complete, remove the filled bottles from the machine.
See also  SOP for Filling Line for Eye Drops

4.3 Post-Operation

  1. Turn off the machine and disconnect it from the power supply.
  2. Clean all contact parts and the surrounding area as per the cleaning procedure.
  3. Record the operation details in the equipment logbook.

4.4 Maintenance

  1. Regularly inspect the machine for wear and tear.
  2. Lubricate moving parts as per the manufacturer’s recommendations.
  3. Perform calibration checks as per the schedule.
  4. Replace any worn-out parts promptly.

5) Abbreviations, if any

None

6) Documents, if any

  1. Equipment logbook
  2. Maintenance record
  3. Calibration record

7) Reference, if any

GMP Guidelines for pharmaceutical production and equipment handling.

8) SOP Version

Version 1.0

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