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SOP for In-Process Friability Testing

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Standard Operating Procedure for in-process Friability Testing

Purpose

The purpose of this SOP is to outline the procedures for conducting friability testing during the tablet manufacturing process to assess the durability and quality of tablets.

Scope

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

Responsibilities

  • Quality Control Analysts: Conducting friability testing according to this SOP.
  • Production Department: Providing samples for testing and cooperating with quality control personnel.
  • Quality Assurance Department: Ensuring compliance with regulatory standards and guidelines.

Procedure

  1. Weigh a predetermined amount of tablets and place them in the friability testing apparatus.
  2. Operate the apparatus according to manufacturer instructions to subject the tablets to mechanical stress.
  3. After the test cycle, remove the tablets and gently remove any loose dust or debris.
  4. Weigh the tablets again and calculate the percentage of weight loss.
  5. Compare the percentage of weight loss against acceptance criteria.
  6. Document all testing procedures, observations, and results accurately and thoroughly.
  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 Blister Pack Integrity Testing

Abbreviations Used

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

Documents

  • Friability 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
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