Standard Operating Procedure for Cleaning Capsule Filling Machines After Batch Completion
Department | Capsule Manufacturing |
---|---|
SOP No. | SOP/CM/111/2025 |
Supersedes | SOP/CM/111/2022 |
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 outline the procedures for cleaning capsule filling machines after the completion of a production batch. Effective cleaning ensures that cross-contamination is prevented, machinery operates efficiently, and compliance with Good Manufacturing Practices (GMP) is maintained.
2. Scope
This SOP applies to all capsule filling machines in the production department. It covers cleaning after the completion of each batch to ensure the equipment is thoroughly cleaned before the next batch is produced.
3. Responsibilities
- Production Operators: Responsible for carrying out the cleaning procedure as outlined in this SOP, ensuring that all equipment components are thoroughly cleaned and documented.
- Maintenance Team: Ensures that any mechanical components that need disassembly for cleaning are properly reassembled and functioning.
- Quality Control (QC) Team: Responsible for verifying that the cleaning process has been completed satisfactorily and that there is no residual contamination left in the equipment.
- Production Supervisor: Oversees the cleaning process, ensures that it is carried out according to the SOP, and ensures that the equipment is fit for the next batch.
4. Accountability
The Capsule Manufacturing Supervisor is accountable for ensuring that the capsule filling machines are properly cleaned according to this SOP and that the cleaning process is documented and reviewed. The Maintenance Team is responsible for ensuring that any necessary repairs or maintenance are completed during cleaning. The QA Manager is responsible for confirming that the cleaning procedure meets all GMP standards.
5. Procedure
5.1 Preparation for Cleaning
Before beginning the cleaning process, the following preparations should be made:
-
Ensure the Machine is Stopped
- Ensure that the machine is turned off and that the power is disconnected to avoid any accidents during cleaning.
-
Gather Cleaning Materials
- Collect all necessary cleaning materials, including water, approved cleaning agents, brushes, lint-free cloths, and any required PPE (Personal Protective Equipment).
- Ensure that cleaning agents are non-corrosive and safe for the capsule filling machine components.
-
Prepare Cleaning Log
- Prepare the Cleaning Log (Annexure-1) where all cleaning actions and observations will be recorded.
5.2 Disassembly of Capsule Filling Machine
If required, the following steps should be followed to disassemble the parts of the capsule filling machine that need cleaning:
-
Remove All Product Contact Parts
- Remove all parts that come into direct contact with the capsule fill, such as the dosing discs, fill plates, hopper, and any tools or feeders.
-
Ensure Proper Labeling of Removed Parts
- Label all disassembled parts clearly to ensure that they are reassembled in the correct order after cleaning.
-
Place Parts in Appropriate Cleaning Stations
- Place all disassembled parts in designated cleaning stations to ensure that the cleaning process is carried out effectively.
5.3 Cleaning Process
Follow these steps to clean the capsule filling machine and its components:
-
Clean All Components
- Use a non-abrasive brush to remove any residual powder or product from the components. Pay special attention to areas that are difficult to reach, such as the hopper and dosing mechanism.
- Wipe all parts with a lint-free cloth to remove any remaining dust, powder, or cleaning solution.
-
Rinse with Water
- Rinse all components with warm water to remove any cleaning solution residues.
- Ensure that all parts are thoroughly rinsed and there are no traces of cleaning chemicals left on any surfaces.
-
Use Approved Cleaning Agents
- Apply approved cleaning agents to remove any sticky or residual substances that cannot be removed with water alone. Follow the manufacturer’s instructions on the use of cleaning agents.
- Ensure that the cleaning agents used are compatible with the machine parts and do not cause damage or degradation of the material.
-
Disinfect All Components
- If required, disinfect the components after cleaning to prevent microbial contamination.
5.4 Drying and Reassembly
After cleaning, the components must be dried and reassembled:
-
Dry All Components
- Ensure that all components are dried thoroughly using a clean, dry, lint-free cloth. Allow components to air dry if necessary.
-
Reassemble the Machine
- Once all components are dry, carefully reassemble the capsule filling machine, following the labels placed during disassembly.
5.5 Post-Cleaning Inspection
After the cleaning process, the following checks should be performed:
-
Inspect for Any Residues
- Visually inspect the machine for any residues of product or cleaning solution. If any residues are found, repeat the cleaning process as necessary.
-
Check the Machine for Proper Assembly
- Ensure that all parts are correctly reassembled and secured before starting the machine.
-
Run a Test Batch
- Run a small test batch to verify that the machine is functioning properly and that no contamination remains from the previous batch.
5.6 Documentation
Ensure all actions related to cleaning are documented properly:
-
Record Cleaning Details
- Document the details of the cleaning process, including date, time, operator, and any issues or deviations in the Cleaning Log (Annexure-1).
-
Record Inspection Results
- 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 filling machine components | No residue found |
Annexure-2: Equipment Inspection Log
Equipment ID | Inspection Date | Inspection Results | Operator | Next Maintenance Due |
---|---|---|---|---|
Filling 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 |
---|---|---|---|---|
Filling Machine 001 | 02/02/2025 | Recalibrated filling system 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 | Updated cleaning procedure and added inspection details | Improved accuracy and compliance | QA Head |