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SOP for Emergency Shutdown and Restart Procedures

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SOP for Emergency Shutdown and Restart Procedures

Standard Operating Procedure for Emergency Shutdown and Restart Procedures

1) Purpose

The purpose of this SOP is to define the steps and protocols for safely shutting down and restarting manufacturing equipment in case of emergencies to protect personnel and minimize equipment damage.

2) Scope

This SOP applies to all personnel involved in emergency response and equipment operation within the pharmaceutical manufacturing facility.

3) Responsibilities

3.1 Emergency Response Team

  • Execute shutdown procedures during emergencies.
  • Coordinate with operations and safety personnel.

3.2 Operations Personnel

  • Follow emergency shutdown protocols as directed.
  • Assist in equipment inspection and restart procedures.
See also  SOP for Visual and Physical Inspection of Syringes and Vials

4) Procedure

4.1 Emergency Shutdown

  1. Activate emergency stop controls or shutdown switches.
  2. Secure hazardous materials and equipment to prevent further risks.
  3. Evacuate personnel to safe assembly points.

4.2 Equipment Inspection

  1. Assess equipment condition post-emergency.
  2. Identify any damage or potential hazards.

4.3 Restart Procedure

  1. Inspect and repair equipment as necessary.
  2. Coordinate restart with maintenance and operations teams.
  3. Perform system checks and verify normal operation.

5) Abbreviations, if any

SOP: Standard Operating Procedure

6) Documents, if any

  • Emergency Response Plan
  • Shutdown and Restart Checklist
  • Equipment Inspection Reports

7) Reference, if any

OSHA 29 CFR 1910.38: Emergency Action Plans
ICH Q9: Quality Risk Management

See also  SOP for Temperature Mapping in Storage Areas

8) SOP Version

Version 1.0

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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
  • 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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