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Ointments: SOP for Handling Emergency Stops in Machines – V 2.0

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SOP for Handling Emergency Stops in Machines – V 2.0

Procedure for Handling Emergency Stops in Machines

Department Production/Engineering/Quality Assurance (QA)/Safety
SOP No. SOP/Ointment/049
Supersedes V 1.0
Page No. Page X of Y
Issue Date [Insert Issue Date]
Effective Date [Insert Effective Date]
Review Date [Insert Review Date]

1. Purpose

The purpose of this Standard Operating Procedure (SOP) is to establish a structured approach for handling emergency stops in machines used in ointment manufacturing. Proper emergency stop procedures ensure personnel safety, prevent equipment damage, and maintain compliance with Good Manufacturing Practices (GMP).

2. Scope

This SOP applies to all personnel involved in operating, maintaining, and monitoring manufacturing machines in the ointment production facility.

3. Responsibilities

  • Production Supervisor: Ensures personnel are trained in emergency stop procedures.
  • Machine Operator: Identifies emergency situations and activates emergency stops.
  • Engineering Technician: Assesses and repairs equipment after an emergency stop.
  • Quality Assurance (QA) Personnel: Verifies GMP compliance and records incidents.
  • Safety Officer: Conducts safety audits and ensures adherence to emergency protocols.
See also  Ointments: SOP for Particle Size Reduction in Ointment Manufacturing - V 2.0

4. Accountability

The Production, Engineering, and QA Managers are accountable for ensuring that emergency stop procedures are followed, recorded, and reviewed regularly.

5. Procedure

5.1 Identifying Emergency Situations

  • Equipment malfunction (e.g., overheating, abnormal noise, or vibration).
  • Operator injury or entrapment.
  • Electrical failure or short circuit.
  • Product leakage or contamination.
  • Fire or chemical spill in the vicinity of the equipment.

5.2 Activating Emergency Stops

  • Press the Emergency Stop Button immediately if an emergency arises.
  • Ensure the machine comes to a complete stop.
  • Alert nearby personnel and supervisors about the situation.
  • Isolate power supply to the affected machine if necessary.

5.3 Post-Emergency Stop Actions

  • Inspect the machine visually for any visible hazards.
  • Verify if the emergency stop was triggered due to a system fault or operator error.
  • Lock out and tag out (LOTO) the equipment to prevent unintended restart.
  • Document the event in the Emergency Stop Log.

5.4 Troubleshooting and Restarting the Machine

5.4.1 Engineering Assessment

  • The Engineering team must inspect the equipment and diagnose the issue.
  • Identify the cause of the emergency stop and implement necessary repairs.
  • Confirm that all safety measures are in place before restarting.
See also  Ointments: SOP for QA Oversight During Packing Operations - V 2.0

5.4.2 QA Verification

  • QA personnel must conduct a post-incident inspection.
  • Ensure no contamination or product loss has occurred.
  • Approve the restart only after compliance verification.

5.4.3 Machine Restart

  • Remove LOTO after Engineering and QA clearance.
  • Ensure the emergency stop button is reset before restarting.
  • Gradually start the machine and monitor for abnormalities.
  • Resume normal production only after confirming stability.

5.5 Reporting and Documentation

  • Record the incident in the Emergency Stop Log (Annexure-1).
  • Conduct a root cause analysis for repeated emergency stops.
  • Implement corrective and preventive actions (CAPA) if necessary.

6. Abbreviations

  • GMP – Good Manufacturing Practices
  • QA – Quality Assurance
  • QC – Quality Control
  • LOTO – Lockout/Tagout
  • CAPA – Corrective and Preventive Action

7. Documents

  • Emergency Stop Log (Annexure-1)
  • Incident Investigation Report (Annexure-2)
See also  Ointments: SOP for Particle Size Analysis in Ointments - V 2.0

8. References

  • WHO GMP Guidelines for Pharmaceutical Manufacturing
  • 21 CFR Part 211 – Current Good Manufacturing Practices
  • OSHA Lockout/Tagout Standard (29 CFR 1910.147)

9. SOP Version

Version 2.0

10. Approval Section

Prepared By Checked By Approved By
Signature
Date
Name
Designation
Department

11. Annexures

Annexure-1: Emergency Stop Log

Date Machine ID Reason for Stop Action Taken Restart Approved By
01/02/2025 EM-101 Overheating Cooling system repaired QA Officer
02/02/2025 EM-102 Product leakage Seal replaced QA Officer

Annexure-2: Incident Investigation Report

Date Machine ID Incident Description Root Cause Corrective Action Verified By
01/02/2025 EM-101 Emergency stop due to overheating Blocked air vents Air vents cleaned QA Head
02/02/2025 EM-102 Leak detected at filling station Defective gasket Gasket replaced QA Head

12. Revision History:

Revision Date Revision No. Details of Revision Reason for Revision Approved By
01/01/2024 1.0 Initial Version New SOP QA Head
01/02/2025 2.0 Updated SOP Format Standardization of Document QA Head
Ointments V 2.0 Tags:Ointment application SOP, Ointment batch record SOP, Ointment compounding SOP, Ointment dispensing SOP, Ointment filling SOP, Ointment formulation SOP, Ointment manufacturing SOP, Ointment microbiological testing SOP, Ointment pH testing SOP, Ointment production SOP, Ointment quality control SOP, Ointment stability study SOP, Pharmaceutical ointment SOP, SOP for ointment homogenization, SOP for ointment labeling, SOP for ointment mixing, SOP for ointment packaging, SOP for ointment preparation, SOP for ointment raw material testing, SOP for ointment shelf-life determination, SOP for ointment stability testing, SOP for ointment sterilization, SOP for ointment storage, SOP for ointment testing, SOP for ointment viscosity testing

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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

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  • 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
  • Ointments V 2.0
  • Raw Material Warehouse V 2.0
  • Tablet Manufacturing V2.0

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