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Quality Assurance: SOP for Viscosity Testing of Gels

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SOP for Viscosity Testing of Gels

Standard Operating Procedure for Viscosity Testing of Gels

1) Purpose

The purpose of this SOP is to establish procedures for viscosity testing of gels in the pharmaceutical industry to ensure consistency and quality control during production.

2) Scope

This SOP applies to all personnel involved in viscosity testing of gels within the pharmaceutical production facility.

3) Responsibilities

Quality Control (QC) Supervisor: Oversee viscosity testing procedures as per this SOP.
QC Analysts: Perform viscosity tests and record results accurately.
Production Operators: Provide gel samples and support as required for viscosity testing.

See also  Quality Assurance: SOP for Recall Procedure for Gels

4) Procedure

4.1 Equipment Setup
4.1.1 Verify and calibrate the viscosity measuring instrument (e.g., viscometer) according to manufacturer instructions.
4.1.2 Prepare required accessories and standards for viscosity measurement.

4.2 Sample Preparation
4.2.1 Allow gel samples to equilibrate to room temperature before testing.
4.2.2 Mix samples gently to ensure homogeneity without introducing air bubbles.

4.3 Viscosity Measurement
4.3.1 Set the viscometer to the appropriate speed and spindle based on the viscosity range of the gel.
4.3.2 Immerse the spindle into the gel sample and start the measurement.
4.3.3 Record viscosity readings once stabilized and repeat measurements as necessary for accuracy.

4.4 Calculation and

Recording
4.4.1 Calculate viscosity values using the appropriate formula or software provided by the manufacturer.
4.4.2 Record viscosity measurements in the designated QC records or electronic systems.

See also  Quality Assurance: SOP for Particle Size Distribution in Gels

4.5 Data Analysis and Acceptance Criteria
4.5.1 Compare viscosity measurements against predefined acceptance criteria or specifications.
4.5.2 Identify and document any deviations from specified viscosity limits.

4.6 Cleaning and Maintenance
4.6.1 Clean the viscometer and accessories thoroughly after each use as per cleaning SOP.
4.6.2 Perform regular maintenance and calibration of the viscometer as per schedule.

5) Abbreviations, if any

SOP: Standard Operating Procedure
QC: Quality Control

6) Documents, if any

– Viscosity Test Reports
– Calibration Certificates
– Equipment Cleaning and Maintenance Logs
– SOP for Viscosity Testing

7) Reference, if any

– USP <911> Viscosity
– Pharmacopoeial guidelines for viscosity testing of pharmaceuticals
– Manufacturer’s instructions for viscometer operation and calibration

See also  SOP for Specific Gravity Testing

8) SOP Version

Version 1.0

Quality Assurance Tags:Analytical Method Development for Gels, Assay of Active Ingredient in Gels, Cleaning Equipment for Gel Production, Contamination Prevention in Gel Manufacturing, Equipment Calibration for Gel Manufacturing, Final Product Inspection for Gels, Gel Formulation Development, Gel Homogeneity Testing, Gel Labeling Procedures, Gel Preparation SOP, Gel Production Documentation, Gel Production Waste Disposal, Gel Quality Control Testing, Gel Viscosity Testing, In-process Testing for Gels, Microbial Testing of Gels, Packaging of Gels, Particle Size Analysis in Gels, Particle Size Distribution in Gels, pH Testing of Gels, Pharmaceutical Gel Manufacturing, Process Optimization for Gel Manufacturing, Process Validation for Gels, Raw Material Inspection for Gels, Rheological Testing in Gels, Sample Collection for Gel Quality Testing, Stability Testing for Gels, Sterility in Gel Production, Storage Conditions for Gels, Training for Gel Production Personnel

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Standard Operating Procedures V 1.0

  • Aerosols
  • Analytical Method Development
  • Bioequivalence Bioavailability Study
  • Capsule Formulation
  • Clinical Studies
  • Creams
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  • Good Distribution Practice
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  • Purchase Departments
  • Quality Assurance
  • Quality Control
  • Raw Material Stores
  • Regulatory Affairs
  • Tablet Manufacturing
  • Rectal Dosage Forms
  • Transdermal Patches
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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
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  • Creams V 2.0
  • Elixers V 2.0
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  • Raw Material Warehouse V 2.0
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