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SOP for Suppository Transfer Conveyor

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SOP for Suppository Transfer Conveyor

Operation and Maintenance of Suppository Transfer Conveyor

1) Purpose

The purpose of this SOP is to outline the procedures for operating and maintaining the suppository transfer conveyor to ensure efficient and safe transfer of suppositories during manufacturing processes.

2) Scope

This SOP applies to all personnel involved in the operation, cleaning, and maintenance of the suppository transfer conveyor in the manufacturing facility.

3) Responsibilities

It is the responsibility of production operators, maintenance staff, and quality control personnel to follow this SOP to ensure proper operation and maintenance of the suppository transfer conveyor.

See also  SOP for Stability Testing

4) Procedure

4.1 Preparation

  1. Ensure the work area and conveyor system are clean and free from any obstructions.
  2. Verify the availability and integrity of suppositories ready for transfer.
  3. Inspect the conveyor system, including belts, rollers, and controls, to ensure they are clean and in good working condition.

4.2 Transfer Process

  1. Start the conveyor system and adjust the speed and direction as per operational requirements.
  2. Load suppositories onto the conveyor system using appropriate handling techniques to prevent damage or contamination.
  3. Monitor the transfer process to ensure smooth and continuous movement of suppositories along the conveyor.

4.3 Cleaning and Maintenance

  1. Stop the conveyor system after completing the transfer operation.
  2. Remove any residual suppositories and debris from the conveyor belts and rollers.
  3. Perform routine maintenance tasks
such as lubrication of moving parts and inspection of conveyor components for wear and tear.

5) Abbreviations, if any

N/A

6) Documents, if any

Batch production record, Cleaning log, Conveyor system specifications

7) Reference, if any

GMP guidelines, Manufacturer’s operating manual for conveyor system

8) SOP Version

Version 1.0

See also  SOP for Batch Record Review and Approval
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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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