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Gel Manufacturing: SOP for Operation and Cleaning of Semi-Automatic Tube Sealing Machine – V 2.0

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Gel Manufacturing: SOP for Operation and Cleaning of Semi-Automatic Tube Sealing Machine – V 2.0

Standard Operating Procedure for Operating and Cleaning the Semi-Automatic Tube Sealing Machine in Gel Manufacturing

Department Gel Manufacturing
SOP No. SOP/GM/156/2025
Supersedes SOP/GM/156/2022
Page No. Page 1 of 12
Issue Date 09/06/2025
Effective Date 11/06/2025
Review Date 09/06/2027

1. Purpose

To provide a detailed procedure for the correct and safe operation and cleaning of the semi-automatic tube sealing machine used in gel packaging, ensuring consistent seal integrity and contamination control.

2. Scope

This SOP is applicable to all semi-automatic tube sealing machines installed in the primary packaging area of the Gel Manufacturing department.

3. Responsibilities

  • Machine Operator: Responsible for routine operation, cleaning, and initial trouble-shooting.
  • Production Supervisor: Ensures the equipment is operated and cleaned as per SOP and production plan.
  • QA Officer:
Verifies line clearance and cleaning status, and documents compliance with SOP.

4. Accountability

Head – Manufacturing is accountable for ensuring SOP adherence, operator training, and maintenance of documentation related to the operation and cleaning of the sealing machine.

5. Procedure

5.1 Pre-Startup Checks

  1. Ensure the machine is clean, dry, and free from any previous product remnants.
  2. Check that the sealing jaws are aligned, clean, and free from wear or residue.
  3. Verify calibration of temperature and pressure gauges as per machine logbook.
  4. Confirm electrical connections and ensure emergency stop functions are active.

5.2 Machine Operation

  1. Switch ON the main power supply and set the appropriate sealing temperature (usually 120–150°C depending on tube type).
  2. Allow the machine to reach the set temperature (observe via digital display or thermometer).
  3. Load pre-filled tubes onto the machine one at a time into the sealing jaws.
  4. Press the foot switch to initiate the sealing cycle.
  5. Once sealing is complete, visually inspect each tube for defects like incomplete sealing, over-sealing, or burn marks.
  6. Rejected tubes should be recorded and segregated for investigation.
  7. Monitor every 30 minutes or 100 tubes for seal quality and document the results in the In-process Check Sheet – Annexure-1.

5.3 Shutdown Procedure

  1. Switch off the heating element and allow it to cool to ambient temperature.
  2. Switch off the main power supply.
  3. Clean the area around the machine and dispose of rejected tubes in designated bins.

5.4 Cleaning Procedure

  1. Ensure power is OFF and machine is cool before cleaning begins.
  2. Use a clean lint-free cloth soaked in 70% IPA to wipe the sealing jaws and contact areas.
  3. Clean external surfaces and foot pedal using a separate sanitized cloth.
  4. Document cleaning activity in the Equipment Cleaning Log – Annexure-2.
  5. If any foreign material or residue is not removed, repeat cleaning and report to maintenance if persistent.

5.5 Preventive Maintenance

  1. Perform preventive maintenance monthly as per Maintenance SOP.
  2. Replace sealing jaws if signs of wear or temperature malfunction occur.
  3. Lubricate moving parts (except jaws) using food-grade lubricants.

6. Abbreviations

  • IPA: Isopropyl Alcohol
  • SOP: Standard Operating Procedure
  • QA: Quality Assurance

7. Documents

  1. Machine Logbook
  2. In-process Check Sheet – Annexure-1
  3. Equipment Cleaning Log – Annexure-2

8. References

  • Operator Manual of Semi-Automatic Tube Sealing Machine
  • Schedule M Guidelines – Primary Packaging

9. SOP Version

Version: 2.0

10. Approval Section

Prepared By Checked By Approved By
Signature
Date
Name
Designation Jr. Production Chemist QA Executive Head – Manufacturing
Department Gel Manufacturing Quality Assurance Manufacturing

11. Annexures

Annexure-1: In-process Check Sheet

Time No. of Tubes Sealed Seal Integrity (Pass/Fail) Remarks Checked By

Annexure-2: Equipment Cleaning Log

Date Time Cleaning Performed By Checked By (QA) Remarks

Revision History

Revision Date Revision No. Change Description Reason Approved By
10/03/2022 1.0 Initial issue New equipment installed QA Head
09/06/2025 2.0 Added preventive maintenance section and new annexures Annual review QA Head
See also  Gel Manufacturing: SOP for Calibration and Maintenance of pH Meter - V 2.0
Gels V 2.0 Tags:gel excipients SOP, gel extrudability SOP, gel formulation process guidelines, gel formulation safety SOP, gel formulation SOP template, gel homogenization SOP, gel ingredient weighing SOP, gel labeling and documentation SOP, gel microbial contamination SOP, gel packaging SOP, gel viscosity measurement SOP, gel viscosity testing SOP, pharmaceutical gel SOP, quality control SOP gel formulations, SOP for carbopol gel formulation, SOP for gel pH adjustment, SOP for gel spreadability test, stability testing SOP gel, standard operating procedure gel preparation, topical gel manufacturing SOP

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Standard Operating Procedures V 1.0

  • Aerosols
  • Analytical Method Development
  • Bioequivalence Bioavailability Study
  • Capsule Formulation
  • Clinical Studies
  • Creams
  • Data Integrity
  • Dental Dosage Forms
  • Drug Discovery
  • Environment, Health and Safety
  • Formulation Development
  • Gels
  • Good Distribution Practice
  • Good Warehousing Practices
  • In-Process Control
  • Injectables
  • Liquid Orals
  • Liposome and Emulsion Formulations
  • Lotions
  • Lyophilized Products
  • Maintenance Dept.
  • Medical Devices
  • Metered-Dose Inhaler
  • Microbiology Testing
  • Nanoparticle Formulation
  • Nasal Spray Formulations
  • Nebulizers
  • Ocular (Eye) Dosage Forms
  • Ointments
  • Otic (Ear) Dosage Forms
  • Pharmacovigilance
  • Powder & Granules
  • Purchase Departments
  • Quality Assurance
  • Quality Control
  • Raw Material Stores
  • Regulatory Affairs
  • Tablet Manufacturing
  • Rectal Dosage Forms
  • Transdermal Patches
  • Vaginal Dosage Forms
  • Validations and Qualifications

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NEW! Revised SOPs – V 2.0

  • Aerosols V 2.0
  • Analytical Method Development V 2.0
  • API Manufacturing V 2.0
  • BA-BE Studies V 2.0
  • Biosimilars V 2.0
  • Capsules V 2.0
  • Creams V 2.0
  • Elixers V 2.0
  • Gels V 2.0
  • Injectables V 2.0
  • Ointments V 2.0
  • Raw Material Warehouse V 2.0
  • Tablet Manufacturing V2.0

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