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In-Process Control: SOP for Tablet Hardness Testing 

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Standard Operating Procedure for Hardness Testing

 

Purpose

The purpose of this SOP is to define the procedures for conducting hardness testing during the tablet manufacturing process to ensure the mechanical strength and integrity of capsules.

Scope

This SOP applies to all personnel involved in tablet manufacturing, specifically those responsible for conducting hardness testing.

Responsibilities

  • Quality Control Analysts: Responsible for conducting hardness testing according to this SOP.
  • Production Department: Providing tablets for testing and cooperating with quality control personnel.
  • Quality Assurance Department: Ensuring compliance with regulatory standards and guidelines.

Procedure

  1. Select a representative sample of tablets according to predefined sampling procedures.
  2. Place each tablet individually between the anvils of the hardness tester.
  3. Apply increasing force until the tablet fractures or deforms.
  4. Record the force required to fracture or deform the capsule.
  5. Compare the hardness values against acceptance criteria.
  6. Document all testing procedures, observations, and results accurately and comprehensively.
  7. Review and approve the test results by authorized personnel.
  8. Initiate corrective actions if deviations from acceptance criteria are identified.
See also  SOP for Blend Uniformity Testing

Abbreviations Used

SOP: Standard Operating Procedure
QC: Quality Control
QA: Quality Assurance

Documents

  • Hardness Testing Protocol
  • Standard Operating Procedures Manual
  • Batch Records
  • Quality Control Reports
  • Deviation Reports

Reference

No specific references are cited for this SOP.

SOP Version

Version 1.0

In-Process Control Tags:Antioxidant Testing, Appearance Inspection, Assay Testing, Batch testing, Blend Homogeneity Testing, Blend Uniformity Testing, Clarity Testing, Coating Thickness Measurement, Compliance testing, Container Closure Integrity Testing, Content Uniformity Testing, Disintegration Testing, Dissolution Profile Analysis, Dissolution Testing, Endotoxin testing, Friability Testing, Granule Size Distribution Analysis, Hardness Testing, In-process control, Leakage Testing, Manufacturing standards, Microbial Testing, Moisture Content Determination, Osmolality Testing, Particle Size Distribution Analysis, pH Testing, Process validation, Quality Assurance, Quality Control, Real-time monitoring, Sterility testing, Uniformity of Dosage Units Testing, Viscosity Testing, Weight Variation Testing

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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

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