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SOP for Ring Packaging Machine

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SOP for Ring Packaging Machine

Operation and Maintenance of Ring Packaging Machine

1) Purpose

The purpose of this SOP is to outline the procedures for operating and maintaining the ring packaging machine to ensure efficient and accurate packaging of rings.

2) Scope

This SOP applies to all personnel involved in the operation, cleaning, and maintenance of the ring packaging machine 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 ring packaging machine.

4) Procedure

4.1 Preparation

  1. Ensure the work area and equipment are clean and sanitized before starting the packaging process.
  2. Verify the availability and integrity of rings ready for packaging.
  3. Inspect the ring packaging machine, including conveyor belts and packaging materials, to ensure they are clean and operational.
See also  SOP for Packaging Material Receipt and Inspection

4.2 Packaging Process

  1. Set up the packaging parameters such as packaging speed, labeling requirements, and batch coding according to product specifications.
  2. Load the rings onto the conveyor belt of the packaging machine and start the packaging process.
  3. Monitor the packaging process to ensure accurate placement of rings into packaging materials.

4.3 Cleaning and Maintenance

  1. Stop the ring packaging machine after completing the packaging batch.
  2. Clean the conveyor belts, packaging area, and change packaging materials as required.
  3. Perform routine maintenance
tasks such as inspection of conveyor motors and lubrication of moving parts.

5) Abbreviations, if any

N/A

6) Documents, if any

Batch production record, Cleaning log, Packaging material specifications

7) Reference, if any

GMP guidelines, Manufacturer’s operating manual for ring packaging machine

8) SOP Version

Version 1.0

See also  SOP for Suppository Inspection Machine
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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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