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SOP for Tablet Polishing Machine

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SOP for Tablet Polishing Machine

Operation and Maintenance of Tablet Polishing Machine

1) Purpose

The purpose of this SOP is to outline the procedures for operating and maintaining the tablet polishing machine to ensure smooth and polished tablet surfaces.

2) Scope

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

4) Procedure

4.1 Preparation

  1. Ensure the work area and equipment are clean and sanitized before starting the polishing process.
  2. Verify the availability and integrity of tablets ready for polishing.
  3. Inspect the tablet polishing machine, including polishing drums and brushes, to ensure they are clean and in good condition.
See also  SOP for Suppository Cooling Tunnel

4.2 Polishing Process

  1. Set up the polishing parameters such as polishing speed, pressure, and duration according to tablet specifications.
  2. Load the tablets into the polishing drums and start the polishing process.
  3. Monitor the polishing process to ensure uniform and polished surfaces of tablets.

4.3 Cleaning and Maintenance

  1. Stop the polishing machine after completing the polishing batch.
  2. Remove tablets from the polishing drums and clean the drums and brushes thoroughly to remove any polishing residues.
  3. Perform preventive maintenance tasks such
as checking brushes, inspecting belts, and lubricating moving parts.

5) Abbreviations, if any

N/A

6) Documents, if any

Batch production record, Cleaning log, Tablet polishing machine specifications

7) Reference, if any

GMP guidelines, Manufacturer’s operating manual for tablet polishing machine

8) SOP Version

Version 1.0

See also  SOP for Cream Manufacturing Vessel
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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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