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Capsule: SOP for Cleaning Capsule Printing Machines – V 2.0

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Capsule: SOP for Cleaning Capsule Printing Machines – V 2.0

Standard Operating Procedure for Cleaning Capsule Printing Machines

Department Capsule Manufacturing
SOP No. SOP/CM/117/2025
Supersedes SOP/CM/117/2022
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 define the procedure for cleaning capsule printing machines used in the production process. Cleaning the printing machines ensures that no printing ink, powder, or other residues remain, preventing contamination and ensuring compliance with Good Manufacturing Practices (GMP).

2. Scope

This SOP applies to all capsule printing machines used in the production of hard gelatin capsules. It covers the cleaning procedure after each production batch to ensure that the printing machine is free of contamination and complies with GMP standards.

3. Responsibilities

  • Production Operators: Responsible for disassembling the printing machine, cleaning the parts, and reassembling it after cleaning as per this SOP.
  • Quality Control (QC) Team: Ensures that the cleaning process has been completed properly and verifies that there are no residues or contaminants left on the machine.
  • Quality Assurance (QA) Team: Ensures that the cleaning process is compliant with GMP standards and reviews the cleaning documentation for completeness and accuracy.
  • Maintenance
Team: Ensures that any necessary mechanical repairs are performed during cleaning and reassembles the equipment properly.
  • Production Supervisor: Oversees the cleaning process, ensures that the machine is reassembled correctly, and ensures that the printing machine is ready for the next production run.
  • 4. Accountability

    The Capsule Manufacturing Supervisor is accountable for ensuring that the capsule printing machines are properly cleaned according to this SOP. The QA Manager is responsible for ensuring that the cleaning process complies with GMP and verifying the cleanliness of the machine.

    5. Procedure

    5.1 Preparation for Cleaning

    Before starting the cleaning process, ensure the following steps are completed:

    1. Turn Off the Machine

      1. Ensure that the printing machine is turned off, and the power supply is disconnected to avoid electrical hazards during cleaning.
    2. Gather Cleaning Materials

      1. Collect the necessary cleaning materials, including warm water, approved cleaning agents, brushes, lint-free cloths, sponges, and appropriate Personal Protective Equipment (PPE) for safety.
      2. Ensure that the cleaning agents used are non-corrosive and safe for the materials of the printing machine.
    3. Prepare Cleaning Log

      1. Ensure the Cleaning Log (Annexure-1) is available to record the cleaning actions, operator name, time, and any deviations during the cleaning process.

    5.2 Disassembling the Capsule Printing Machine

    If necessary, disassemble the machine parts to ensure proper cleaning:

    1. Remove Components for Cleaning

      1. Carefully remove parts such as ink rollers, printing heads, belts, and trays. These components should be handled carefully to avoid damage.
    2. Label Disassembled Parts

      1. Label each disassembled part to ensure proper reassembly after cleaning.
    3. Place Parts in Cleaning Stations

      1. Place all removed components in the designated cleaning stations for proper washing and cleaning.

    5.3 Cleaning Process

    Follow these steps to clean the capsule printing machine:

    1. Initial Rinse

      1. Rinse the capsule printing machine and its components with warm water to remove any printing ink, dust, and debris.
      2. Ensure all surfaces, including internal parts, are rinsed thoroughly.
    2. Apply Cleaning Agents

      1. Apply an approved, mild, non-abrasive cleaning agent to the surfaces of the machine and its components. Use brushes to scrub surfaces and remove any residual ink or debris.
    3. Rinse with Warm Water

      1. Rinse all machine parts thoroughly with warm water to remove all cleaning agents and residues.
      2. Ensure that no cleaning chemicals remain on any part of the machine.
    4. Disinfect (If Required)

      1. If required, apply an appropriate disinfectant to all machine components to prevent microbial contamination. Follow the disinfectant’s instructions for proper use and dilution.
    5. Final Rinse

      1. Perform a final rinse with warm water to ensure that all disinfectant and cleaning agents are removed.

    5.4 Drying and Reassembly

    After cleaning, proceed with drying and reassembling the equipment:

    1. Dry the Components

      1. Dry all cleaned components with a clean, dry, lint-free cloth. Allow parts to air dry if necessary.
    2. Reassemble the Equipment

      1. After drying, carefully reassemble the printing machine, ensuring all parts are correctly reinstalled following the labels placed during disassembly.

    5.5 Post-Cleaning Inspection

    Once the cleaning and reassembly are complete, perform the following checks:

    1. Inspect for Residual Contamination

      1. Visually inspect the machine for any remaining cleaning agents, ink, or other contaminants. If contamination is found, repeat the cleaning process.
    2. Check for Proper Reassembly

      1. Ensure that all components are properly reassembled and secure.
    3. Run Test Batch

      1. Run a small test batch of capsules to ensure that the printing machine is working correctly and that no contamination remains from the previous batch.

    5.6 Documentation

    Document the entire cleaning process for compliance and traceability:

    1. Complete Cleaning Log

      1. Record all cleaning actions, including the cleaning date, operator, actions taken, and any issues or observations in the Cleaning Log (Annexure-1).
    2. Post-Cleaning Inspection

      1. Document 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

    1. Cleaning Log (Annexure-1)
    2. Equipment Inspection Log (Annexure-2)
    3. 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 printing machine components No residue found

    Annexure-2: Equipment Inspection Log

    Equipment ID Inspection Date Inspection Results Operator Next Maintenance Due
    Printing 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
    Printing Machine 001 02/02/2025 Recalibrated ink dispensing 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 post-cleaning inspection steps Improved cleaning process accuracy QA Head
    See also  Capsule: SOP for Adjusting Capsule Sealing Machine Parameters - V 2.0
    Capsules V 2.0 Tags:Active pharmaceutical ingredients (APIs) Capsule excipients, Capsule batch records, Capsule cleaning procedures, Capsule content uniformity, Capsule deviation management, Capsule disintegration testing, Capsule dissolution testing, Capsule filling process, Capsule inspection techniques, Capsule labeling requirements, Capsule maintenance protocols, Capsule Manufacturing, Capsule manufacturing equipment, Capsule packaging standards, Capsule process validation, Capsule production scheduling, Capsule Quality Control, Capsule regulatory compliance, Capsule safety guidelines, Capsule sealing methods, Capsule size specifications, Capsule stability testing, Capsule storage conditions, Capsule training programs, Empty capsule shells, Hard gelatin capsules, Pharmaceutical capsules, Soft gelatin capsules, Vegetarian capsules

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    Standard Operating Procedures V 1.0

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