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SOP for Tablet Compression Tool

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SOP for Tablet Compression Tool

Operation and Maintenance of Tablet Compression Tool

1) Purpose

The purpose of this SOP is to outline the procedures for operating and maintaining the tablet compression tool to ensure consistent and quality tablet production during the manufacturing process.

2) Scope

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

See also  SOP for Media Fill Studies

4) Procedure

4.1 Preparation

  1. Ensure the work area and equipment are clean and sanitized before starting the compression process.
  2. Verify the availability and integrity of tablet formulations ready for compression.
  3. Inspect the tablet compression tool, including punches, dies, and controls, to ensure they are clean and in good working condition.

4.2 Compression Process

  1. Set up the tablet compression tool as per the specifications of the tablet batch.
  2. Adjust machine settings such as compression force and speed according to the tablet formulation requirements.
  3. Start the compression process and monitor tablet quality and uniformity.

4.3 Cleaning and Maintenance

  1. Stop the compression process after completing the batch.
  2. Remove punches and dies from the tool and clean them thoroughly using approved cleaning agents.
  3. Inspect and clean all
parts of the compression tool to remove any residue or contaminants.

5) Abbreviations, if any

N/A

6) Documents, if any

Batch production record, Cleaning log, Tablet compression tool specifications

7) Reference, if any

GMP guidelines, Manufacturer’s operating manual for tablet compression tool

8) SOP Version

Version 1.0

See also  SOP for Tablet Counting 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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