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SOP for Tablet Friability Testing

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SOP for Tablet Friability Testing

Procedure for Tablet Friability Testing

1) Purpose

The purpose of this SOP is to outline the procedure for determining the friability of tablets to ensure they have adequate mechanical strength to withstand handling and transportation.

2) Scope

This SOP applies to all tablet batches produced within the manufacturing facility.

3) Responsibilities

Quality Control (QC) Department: Responsible for conducting friability testing and ensuring compliance with this SOP.
Production Department: Responsible for providing tablet samples for testing and maintaining process parameters.

4) Procedure

4.1 Sampling:
    4.1.1 Collect a representative sample of tablets from different locations within a batch according to the sampling plan.
    4.1.2 Ensure the sample size is adequate (e.g., 20 tablets) to obtain a uniform representation.

See also  SOP for Particulate Matter Testing in Liquids

4.2 Equipment Preparation:
    4.2.1 Calibrate the friability tester as per the manufacturer’s instructions.
    4.2.2 Ensure the tester is clean and free from previous residues.

4.3 Friability Testing Procedure:
    4.3.1 Weigh the sample of tablets and record the initial weight.
    4.3.2 Place the tablets in the drum of the friability tester.
    4.3.3 Operate the tester for a specified number of rotations (e.g., 100 rotations at 25 rpm).
    4.3.4 After testing, remove the tablets and brush off any dust.
    4.3.5 Weigh the tablets again and record the final weight.

4.4 Calculation:
    4.4.1 Calculate

the friability using the formula: Friability (%) = [(Initial Weight – Final Weight) / Initial Weight] × 100.
    4.4.2 Assess the friability result to determine if it meets the acceptance criteria.

See also  SOP for Grittiness Testing in Topical Preparations

4.5 Acceptance Criteria:
    4.5.1 The tablet batch is acceptable if the friability is less than or equal to 1.0%.

4.6 Documentation:
    4.6.1 Document all results and calculations in the Tablet Friability Test Record.
    4.6.2 Review and approve the documentation by QC Manager.

5) Abbreviations, if any

QC: Quality Control

6) Documents, if any

Tablet Friability Test Record
Calibration Record for Friability Tester
Sampling Plan Document

7) Reference, if any

USP <1216> – Tablet Friability
21 CFR Part 211 – Current Good Manufacturing Practice for Finished Pharmaceuticals

8) SOP Version

Version 1.0

In-Process Control Tags:Blend uniformity testing SOP, Bulk density testing SOP, Capsule content uniformity SOP, Capsule disintegration testing SOP, Capsule dissolution testing SOP, Capsule weight variation SOP, Clarity and opalescence testing of liquids SOP, Endotoxin testing in injectable products SOP, Flowability testing of powders SOP, Granulation size distribution SOP, Moisture content determination in granules SOP, Osmolality testing SOP, Particulate matter testing in liquids SOP, pH measurement of solutions SOP, Pyrogen testing SOP, Specific gravity testing of liquids SOP, Sterility testing SOP, Tablet disintegration testing SOP, Tablet dissolution testing SOP, Tablet friability testing SOP, Tablet hardness testing SOP, Tablet thickness measurement SOP, Tablet weight variation SOP, Uniformity of dosage units SOP, Viscosity testing of liquids SOP

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Next Post: SOP for Moisture Content Control: Monitoring and Controlling Moisture Levels in Capsules to Prevent Issues with Stability or Dissolution

Standard Operating Procedures V 1.0

  • Aerosols
  • Analytical Method Development
  • Bioequivalence Bioavailability Study
  • Capsule Formulation
  • Clinical Studies
  • Creams
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  • Regulatory Affairs
  • Tablet Manufacturing
  • Rectal Dosage Forms
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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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