Skip to content
  • Clinical Studies
  • Pharma GMP
  • Pharma Tips
  • Stability Studies
  • Pharma Books
  • Schedule M

SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

  • Home
  • Job Safety Analysis (JSA)
    • Oral Dosage Forms (Tablets & Capsules)
    • Oral Liquid Dosage Forms (Syrups, Elixirs, Suspensions, Emulsions)
    • Powder and Granule Dosage Forms
    • Topical Dosage Forms (Creams, Ointments, Gels, Lotions, Pastes)
    • Transdermal Dosage Forms (Patches)
  • Standard Test Procedures (STP)
  • SOP – Blog Post
  • Toggle search form

SOP for Conducting Emergency Shutdown of Equipment

Posted on By

SOP for Conducting Emergency Shutdown of Equipment

Standard Operating Procedure for Conducting Emergency Shutdown of Equipment

1) Purpose

The purpose of this SOP is to provide a structured procedure for safely and efficiently shutting down equipment during emergencies to protect personnel, prevent damage, and mitigate risks to the facility and environment.

2) Scope

This SOP applies to all employees, contractors, and emergency response team (ERT) members involved in the operation and maintenance of equipment across manufacturing, laboratory, and storage facilities.

3) Responsibilities

  • Emergency Response Team (ERT): Execute and supervise emergency shutdown procedures.
  • Supervisors: Ensure personnel are trained on emergency shutdown protocols and manage the shutdown process within their departments.
  • Operators: Perform shutdown procedures as outlined in this SOP and notify supervisors during emergencies.
  • Maintenance Team: Inspect equipment post-shutdown and ensure safe reactivation.
  • Safety Officers: Monitor compliance with shutdown protocols and assess risks during emergencies.

4) Procedure

4.1 Identifying Emergency Scenarios Requiring Shutdown

  1. Critical Scenarios:
    • Fire or explosion near operational equipment.
    • Chemical leaks or spills in equipment areas.
    • Power outages or electrical surges.
    • Mechanical malfunctions posing immediate hazards.
    • Natural disasters (earthquakes, floods).
  2. less
    Copy code

  3. Initial Assessment:
    • Operators and supervisors must assess the severity of the situation and decide whether a full or partial shutdown is necessary.
See also  SOP for Documenting Routine EHS Audits

4.2 Emergency Shutdown Steps

  1. Notify Personnel:
    • Immediately alert all personnel in the vicinity of the affected equipment
using alarms or verbal communication.
  • Ensure non-essential personnel evacuate the area.
  • less
    Copy code

  • Power Down Equipment:
    • Deactivate equipment using the designated emergency stop button or power switch.
    • Isolate equipment from the main power supply by switching off circuit breakers, if required.
  • Contain Associated Risks:
    • For equipment handling hazardous materials, close all valves and seals to prevent leaks.
    • Activate emergency containment systems, such as spill containment trays or gas absorption units.
  • Engage Safety Systems:
    • Activate fire suppression or ventilation systems, if available, to mitigate secondary hazards.
  • Document Shutdown Actions:
    • Log all actions taken during the shutdown in the Emergency Shutdown Log (Annexure 1).
  • 4.3 Post-Shutdown Activities

    1. Verify Safety:
      • Ensure the area is safe for personnel reentry by conducting air quality checks and visual inspections.
      • Confirm that all equipment is powered off and deactivated.
    2. less
      Copy code

    3. Inspect Equipment:
      • Maintenance teams must inspect equipment for damage and identify any necessary repairs.
      • Record inspection findings in the Equipment Inspection Report (Annexure 2).
    4. Incident Reporting:
      • Document the incident details, including the cause, affected equipment, and response actions, in the Emergency Incident Log (Annexure 3).
    5. Notify Regulatory Authorities:
      • If required by law, report the incident and shutdown actions to regulatory bodies.

    4.4 Restarting Equipment

    1. Pre-Restart Checks:
      • Verify that all repairs and maintenance activities are complete.
      • Ensure the area is free of hazards and all safety systems are functional.
    2. less
      Copy code

    3. Gradual Restart:
      • Follow standard operating procedures for equipment startup, monitoring for irregularities.
      • Test equipment performance under supervision before resuming full operations.

    4.5 Training and Preparedness

    1. Employee Training:
      • Conduct annual training sessions for operators on emergency shutdown procedures.
    2. less
      Copy code

    3. Drills:
      • Perform emergency shutdown drills quarterly to evaluate response time and procedural compliance.
      • Record drill outcomes in the Emergency Drill Log (Annexure 4).
    4. Equipment Maintenance:
      • Ensure emergency stop buttons and associated safety systems are inspected monthly and maintained in working condition.

    5) Abbreviations, if any

    • ERT: Emergency Response Team
    • PPE: Personal Protective Equipment

    6) Documents, if any

    • Emergency Shutdown Log
    • Equipment Inspection Report
    • Emergency Incident Log
    • Emergency Drill Log

    7) Reference, if any

    • OSHA Lockout/Tagout Standards
    • NFPA Standards for Fire Protection
    • ISO 45001 Occupational Health and Safety Management

    8) SOP Version

    Version: 1.0

    Annexure

    Template 1: Emergency Shutdown Log

     
    Date Equipment Name Shutdown Time Actions Taken Performed By
    DD/MM/YYYY Reactor Unit A 10:00 AM Power Off, Valves Sealed John Doe

    Template 2: Equipment Inspection Report

     
    Date Equipment Name Inspection Findings Action Taken Inspector Name
    DD/MM/YYYY Boiler Unit B Minor Valve Leak Valve Replaced Jane Smith

    Template 3: Emergency Drill Log

     
    Date Drill Type Duration Observations Improvement Actions
    DD/MM/YYYY Shutdown Drill 15 Minutes Delayed Operator Response Additional Training Scheduled
    See also  SOP for Managing Waste During Emergency Shutdowns
    Environment, Health and Safety Tags:Emergency response for hazardous materials incidents, Hazardous materials classification, Hazardous materials compliance audits, Hazardous materials decontamination procedures, Hazardous materials disposal methods, Hazardous materials emergency planning, Hazardous materials emergency response guidebook, Hazardous materials exposure limits, Hazardous materials handling, Hazardous materials handling equipment, Hazardous materials incident command system, Hazardous materials incident reporting, Hazardous materials inventory management, Hazardous materials labeling requirements, Hazardous materials monitoring equipment, Hazardous materials packaging requirements, Hazardous materials placarding requirements, Hazardous materials regulatory agencies, Hazardous materials response team training, Hazardous materials risk assessment, Hazardous materials security plans, Hazardous materials shipping papers, Hazardous materials spill response, Hazardous materials storage guidelines, Hazardous materials training requirements, Hazardous materials transportation regulations, Hazardous materials transportation safety, Personal protective equipment for hazardous materials, Regulatory compliance in hazardous materials management, Safety procedures for hazardous materials

    Post navigation

    Previous Post: Tablets: SOP for End-Point Determination in Granulation Process – V 2.0
    Next Post: SOP for Conducting Exploratory Toxicology Studies

    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

    Read SOPs in your Language:

     - 
    Bengali
     - 
    bn
    English
     - 
    en
    Gujarati
     - 
    gu
    Hindi
     - 
    hi
    Malayalam
     - 
    ml
    Marathi
     - 
    mr
    Punjabi
     - 
    pa
    Tamil
     - 
    ta
    Telugu
     - 
    te

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

    New Publication: A must for All.

    Copyright © 2025 SOP Guide for Pharma.

    Powered by PressBook WordPress theme

    Go to mobile version