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

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 Cleaning and Maintenance of Inspection Equipment

Posted on By

Standard Operating Procedure for Cleaning and Maintenance of Inspection Equipment

1. Purpose

The purpose of this Standard Operating Procedure (SOP) is to establish guidelines for the systematic cleaning and maintenance of inspection equipment to ensure its accuracy, reliability, and optimal performance during quality control activities. This SOP aims to prevent contamination, reduce downtime, and extend the lifespan of inspection equipment.

2. Scope

This SOP applies to all personnel involved in the cleaning and maintenance of inspection equipment, including operators, technicians, and quality assurance staff, in the quality control department.

3. Responsibilities

  • Inspection Equipment Operator: Responsible for conducting routine cleaning of the inspection equipment as per this SOP and reporting any equipment issues to the supervisor.
  • Quality Control (QC) Technician: Responsible for performing scheduled maintenance checks and repairs of inspection equipment as required.
  • Quality Assurance (QA) Staff: Responsible for verifying compliance with this SOP and ensuring that the inspection equipment is functioning accurately and properly maintained.
See also  SOP for Cleaning and Maintenance of Thickness Sorting Equipment

4. Procedure

4.1 Cleaning of Inspection Equipment:

  • Ensure that the inspection equipment is turned off and disconnected from the power source before cleaning.
  • Use clean, lint-free, and non-abrasive materials, such as microfiber cloths, to wipe the exterior surfaces of the equipment.
  • For sensitive optical components and lenses, use approved cleaning solutions and follow the manufacturer’s cleaning instructions to
prevent damage.
  • Clean any removable parts, such as trays and holders, separately using suitable cleaning agents, and ensure they are dry and free from residues before reassembling.
  • Dispose of any waste generated during the cleaning process according to the company’s waste disposal procedures.
  • 4.2 Maintenance of Inspection Equipment:

    • Develop a maintenance schedule for inspection equipment based on the manufacturer’s recommendations and historical performance data.
    • Perform routine maintenance checks, such as lubrication of moving parts, alignment checks, and calibration verification, as specified in the maintenance schedule.
    • Keep a log of all maintenance activities, including the date, type of maintenance performed, and the personnel responsible.
    • If any equipment issues are identified during maintenance checks, report them to the QC technician or supervisor for further assessment and repair.
    • Coordinate with the QC technician to conduct major repairs and overhaul of the inspection equipment as needed.

    5. Abbreviations

    SOP: Standard Operating Procedure
    QC: Quality Control
    QA: Quality Assurance

    6. Documents

    The following documents are relevant to this SOP:

    • Inspection Equipment Cleaning Procedure
    • Inspection Equipment Maintenance Schedule
    • Maintenance Log for Inspection Equipment

    7. References

    No specific external references are required for this SOP as it is based on internal company procedures and industry best practices.

    8. SOP Version

    This is version 1.0 of the SOP for Cleaning and Maintenance of Inspection Equipment, effective as of [Insert Date].

    See also  SOP for Operation of Tablet Thickness Sorter
    Tablet Manufacturing Tags:Tablet batch record review, Tablet blending SOP, Tablet cleaning and maintenance, Tablet coating procedure, Tablet compression SOP, Tablet disintegration test procedure, Tablet dissolution procedure, Tablet formulation SOP, Tablet friability testing SOP, Tablet labeling and packaging SOP, Tablet manufacturing equipment SOP, Tablet manufacturing SOP, Tablet packaging SOP, Tablet production procedure, Tablet quality control SOP, Tablet sampling and in-process testing SOP, Tablet stability testing SOP, Tablet storage and handling procedure, Tablet uniformity testing procedure, Tablet weight variation SOP

    Post navigation

    Previous Post: SOP for Tablet Inspection Process
    Next Post: SOP for Handling and Rejection of Defective Tablets

    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