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 Operation of Bottle and Cap Conveyors

Posted on By

Standard Operating Procedure for Operation of Bottle and Cap Conveyors

1. Purpose

The purpose of this Standard Operating Procedure (SOP) is to outline the procedure for the proper operation of bottle and cap conveyors in pharmaceutical manufacturing. This ensures the efficient and safe transportation of bottles and caps while maintaining compliance with Good Manufacturing Practices (GMP).

2. Scope

This SOP applies to all personnel involved in the operation of bottle and cap conveyors within the pharmaceutical manufacturing facility.

3. Responsibilities

  • Conveyor Operator: Responsible for following the procedures outlined in this SOP during conveyor operations.
  • Supervisor: Oversees and verifies compliance with this SOP, including training and documentation.

4. Procedure

4.1. Pre-Operation Checks

  1. Inspect the bottle and cap conveyors for any visible damage, misalignments, or defects. Report any issues to the supervisor.
  2. Ensure that the conveyors are clean and free from any residues or contaminants from previous operations.
  3. Verify that all necessary utilities (e.g., electricity, compressed air) are available and functioning properly.
See also  SOP for Operation of ROPP Cap Sealing Machine

4.2. Set-Up

  1. Position the bottle and cap conveyors in the designated locations for operation, ensuring proper alignment.
  2. Adjust conveyor speeds, guides, and other settings as needed to accommodate the size and type of bottles and caps to be transported.

4.3. Conveyor Operation

  1. Start the conveyors according to the manufacturer’s instructions and the parameters specified in the batch
record or production plan.
  • Feed bottles and caps onto the conveyors, ensuring proper orientation and spacing to prevent jams or blockages.
  • Monitor the conveyor operation closely to ensure the efficient and safe transportation of bottles and caps.
  • Check for any jams, misalignments, or conveyor stoppages and take corrective action as necessary.
  • Record any operational issues, stoppages, or deviations from the standard procedure.
  • 4.4. Post-Operation Checks

    1. Stop the conveyors when the transportation of bottles and caps is completed or as directed by the supervisor.
    2. Perform visual inspections of the transported bottles and caps to ensure they are in good condition and have not been damaged during transportation.
    3. Segregate and label any damaged or rejected items for further evaluation or disposal.

    4.5. Cleaning and Maintenance

    1. Clean the conveyors and associated equipment after use, following the cleaning procedure.
    2. Perform routine maintenance as per the manufacturer’s recommendations to ensure the continued performance of the conveyors.

    4.6. Documentation

    Properly document all aspects of the conveyor operation, including pre-operation checks, settings, operational issues, and post-operation checks. Maintain records in a secure and accessible location for regulatory inspection.

    5. Abbreviations

    • GMP: Good Manufacturing Practices

    6. Reference

    [Insert any relevant references or standards applicable to the operation of bottle and cap conveyors in the pharmaceutical industry.]

    7. SOP Version

    This is version 1.0 of the “Operation of Bottle and Cap Conveyors SOP,” issued on [insert issuance date].

    See also  SOP for Operation of Colloidal Mill
    Liquid Orals Tags:Batch documentation for oral liquids, GMP for liquid orals, Liquid dosage form guidelines, Liquid oral batch release, Liquid oral manufacturing SOP, Liquid oral pharmaceutical facility, liquid oral pharmaceutical SOPs, Liquid oral process validation, Liquid oral product testing, Liquid oral storage conditions, Oral liquid labeling requirements, Oral solution quality assurance, Oral solution SOP, Oral suspension procedure, Packaging of liquid orals, Pharmaceutical liquid dosage SOP, Pharmaceutical liquid formulations, Quality control in liquid oral production, Regulatory compliance for liquid oral products, SOP for flavoring in oral liquids, SOP for syrup manufacturing

    Post navigation

    Previous Post: SOP for Operation of Label Inspection System
    Next Post: SOP for Operation of Shrink Wrapping Machine

    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