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SOP for Equipment Decommissioning

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SOP for Equipment Decommissioning

Standard Operating Procedure for Equipment Decommissioning

1) Purpose

The purpose of this SOP is to outline procedures for the decommissioning of equipment used in the manufacturing of dental dosage forms, ensuring that equipment is safely removed from service, properly disposed of, and documented in compliance with regulatory requirements.

2) Scope

This SOP applies to all equipment used in the production, testing, and control of dental pastes, gels, and mouthwashes within the pharmaceutical industry, where equipment decommissioning is necessary due to obsolescence, replacement, or regulatory reasons.

3) Responsibilities

The Engineering Department is responsible for coordinating and overseeing equipment decommissioning activities. Quality Assurance (QA) personnel are responsible for reviewing and approving decommissioning protocols and documentation. Production personnel are responsible for ensuring equipment readiness for decommissioning.

See also  SOP for Supplier Qualification for Equipment

4) Procedure

4.1 Preparation for Decommissioning

4.1.1 Identify equipment to be decommissioned based on operational status, regulatory requirements, and company policies.

4.1.2 Notify relevant stakeholders, including QA, production, and maintenance departments, about the planned decommissioning activities.

4.2 Decommissioning Process

4.2.1 Disconnect and isolate the equipment from all utilities, including electrical, water, and air supplies.

4.2.2 Drain and purge equipment of all residual materials and substances, following approved procedures for waste disposal.

4.2.3 Remove and label all critical components, parts, and accessories for potential reuse or disposal.

4.3 Cleaning and

Decontamination

4.3.1 Clean and decontaminate equipment surfaces using approved cleaning agents and disinfectants to ensure removal of contaminants and residues.

See also  SOP for Training Documentation for Equipment Use

4.3.2 Perform environmental monitoring and sampling, if required, to verify cleanliness and decontamination efficacy.

4.4 Documentation and Disposal

4.4.1 Complete decommissioning documentation, including decommissioning reports, checklists, and disposal certificates.

4.4.2 Dispose of decommissioned equipment components, parts, and accessories according to environmental regulations and company policies.

4.5 Equipment Disposal Verification

4.5.1 Verify proper disposal of equipment and related materials through documentation review and inspection.

4.5.2 Obtain QA approval for decommissioning reports and disposal certificates before final closure of decommissioning activities.

5) Abbreviations, if any

SOP – Standard Operating Procedure

QA – Quality Assurance

6) Documents, if any

Decommissioning Plan

Decommissioning Checklist

See also  SOP for Noise Level Monitoring of Equipment

Decommissioning Report

Disposal Certificates

7) Reference, if any

Regulatory guidelines for equipment decommissioning

Company-specific decommissioning policies and procedures

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
  • 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.

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