Standard Operating Procedure for Cleaning Capsule Sealing Machines
Department | Capsule Manufacturing |
---|---|
SOP No. | SOP/CM/114/2025 |
Supersedes | SOP/CM/114/2022 |
Page No. | Page 1 of 6 |
Issue Date | 01/02/2025 |
Effective Date | 05/02/2025 |
Review Date | 01/02/2026 |
1. Purpose
The purpose of this SOP is to establish the procedures for cleaning capsule sealing machines after each batch of capsules has been sealed. Effective cleaning of the sealing machine ensures that no residual contaminants, sealing materials, or gelatin remain, preventing cross-contamination and ensuring compliance with Good Manufacturing Practices (GMP).
2. Scope
This SOP applies to all capsule sealing machines used in the production of hard gelatin capsules. It covers the cleaning procedure after each batch to ensure the machines are free from any contamination, which could affect the quality of subsequent batches.
3. Responsibilities
- Production Operators: Responsible for performing the cleaning procedure as outlined in this SOP, including disassembling parts if necessary, cleaning the machine, and reassembling it.
- Maintenance Team: Ensures that the sealing machine is in good working condition, performs any necessary repairs during cleaning, and reassembles components after cleaning.
- Quality Control (QC) Team: Verifies that the cleaning process has been carried out effectively and ensures that there are no residues or contaminants left in the equipment.
- Quality Assurance (QA) Team: Ensures that the cleaning process complies with GMP standards and that documentation is complete and accurate.
- Production Supervisor: Oversees the cleaning process, ensures that the machine is reassembled properly, and verifies that the machine is ready for the next batch of capsules.
4. Accountability
The Capsule Manufacturing Supervisor is accountable for ensuring that the capsule sealing machines are cleaned in accordance with this SOP. The Maintenance Team is responsible for any necessary repairs or maintenance during cleaning. The QA Manager ensures that the cleaning process is in compliance with GMP standards and verifies that all necessary documentation is maintained.
5. Procedure
5.1 Preparation for Cleaning
Before beginning the cleaning process, the following preparations should be made:
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Turn Off the Machine
- Ensure that the capsule sealing machine is turned off and that the power supply is disconnected to avoid accidents during cleaning.
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Gather Cleaning Materials
- Collect the required cleaning materials, including warm water, approved cleaning agents, brushes, lint-free cloths, sponges, and any required Personal Protective Equipment (PPE).
- Ensure that all cleaning agents used are safe for the sealing machine’s components and are non-corrosive.
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Prepare Cleaning Log
- Prepare the Cleaning Log (Annexure-1) to record the cleaning actions, time, operator, and any observations or deviations encountered during the process.
5.2 Disassembling the Capsule Sealing Machine
If necessary, disassemble parts of the sealing machine to ensure thorough cleaning:
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Remove Sealing Components
- Carefully remove the sealing components, such as the sealing wheels, plates, and any other parts that come into direct contact with the capsules during the sealing process.
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Label Disassembled Parts
- Label each disassembled part to ensure that they are reassembled correctly after cleaning.
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Place Parts in Cleaning Stations
- Place all disassembled components in designated cleaning stations where they will be cleaned effectively.
5.3 Cleaning Process
Follow the steps below to clean the capsule sealing machine:
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Initial Rinse
- Rinse the capsule sealing machine and all its components with warm water to remove any gelatin residue or sealing material.
- Ensure that all areas, including those hard to reach, are properly rinsed.
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Apply Cleaning Agents
- Apply a non-abrasive, approved cleaning agent to all surfaces of the machine and components.
- Use brushes or sponges to scrub surfaces, ensuring that no residue remains on any part of the machine.
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Rinse with Warm Water
- Rinse all components thoroughly with warm water to remove all cleaning agents and residues.
- Ensure that no cleaning chemicals are left behind.
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Disinfect (If Required)
- If required, apply an appropriate disinfectant to all machine surfaces to prevent microbial contamination.
- Ensure that the disinfectant is suitable for use on capsule sealing machines and is used in accordance with the manufacturer’s guidelines.
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Final Rinse
- Perform a final rinse with warm water to ensure no disinfectant or cleaning agents remain on the equipment.
5.4 Drying and Reassembly
After the cleaning process, proceed with drying and reassembly:
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Dry the Components
- Dry all cleaned components with a clean, dry, lint-free cloth. Allow components to air dry if necessary.
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Reassemble the Equipment
- Once the components are dry, carefully reassemble the capsule sealing machine, ensuring that all parts are properly secured and aligned.
5.5 Post-Cleaning Inspection
After cleaning and reassembly, perform the following checks:
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Inspect for Residual Contamination
- Visually inspect all parts of the sealing machine for any remaining residues of sealing material, gelatin, or cleaning agents. If any residue is found, repeat the cleaning process.
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Check for Proper Reassembly
- Ensure that all components are correctly reassembled and secure before starting the machine.
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Run a Test Batch
- Run a small test batch of capsules to ensure that the sealing machine is functioning properly and no contamination remains from the previous batch.
5.6 Documentation
Document the cleaning process for compliance and traceability:
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Record Cleaning Details
- Document all cleaning actions, including the cleaning date, operator, actions taken, and any deviations observed in the Cleaning Log (Annexure-1).
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Record Post-Cleaning Inspection
- Record the results of the post-cleaning inspection in the Equipment Inspection Log (Annexure-2).
6. Abbreviations
- SOP: Standard Operating Procedure
- GMP: Good Manufacturing Practice
- QC: Quality Control
- QA: Quality Assurance
- PPE: Personal Protective Equipment
7. Documents
- Cleaning Log (Annexure-1)
- Equipment Inspection Log (Annexure-2)
- Maintenance Log (Annexure-3)
8. References
- USP <1163> – Pharmaceutical Dosage Forms: Capsules
- FDA Guidelines for Capsule Manufacturing
- Good Manufacturing Practice (GMP) Guidelines
9. SOP Version
Version: 2.0
10. Approval Section
Prepared By | Checked By | Approved By | |
---|---|---|---|
Signature | |||
Date | |||
Name | |||
Designation | |||
Department |
11. Annexures
Annexure-1: Cleaning Log
Batch ID | Cleaning Date | Operator | Cleaning Action | Comments |
---|---|---|---|---|
Batch 001 | 02/02/2025 | John Doe | Disassembled and cleaned capsule sealing machine components | No residue found |
Annexure-2: Equipment Inspection Log
Equipment ID | Inspection Date | Inspection Results | Operator | Next Maintenance Due |
---|---|---|---|---|
Sealing Machine 001 | 02/02/2025 | No defects found, machine fully operational | Jane Smith | 02/02/2026 |
Annexure-3: Maintenance Log
Equipment ID | Maintenance Date | Maintenance Activity | Performed By | Next Maintenance Due |
---|---|---|---|---|
Sealing Machine 001 | 02/02/2025 | Recalibrated sealing pressure and cleaned internal components | John Doe | 02/02/2026 |
Revision History:
Revision Date | Revision No. | Revision Details | Reason for Revision | Approved By |
---|---|---|---|---|
01/01/2024 | 1.0 | Initial version | New SOP Creation | QA Head |
01/02/2025 | 2.0 | Added inspection and reassembly details | Improved cleaning process accuracy | QA Head |