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Elixir Department: SOP for Viscosity Comparison Between Batches – V 2.0

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Elixir Department: SOP for Viscosity Comparison Between Batches – V 2.0

Standard Operating Procedure for Viscosity Comparison Between Batches of Elixir Formulations

Department Elixir Department
SOP No. SOP/ELX/226/2025
Supersedes SOP/ELX/226/2022
Page No. Page 1 of 8
Issue Date 11/04/2025
Effective Date 15/04/2025
Review Date 11/04/2026

1. Purpose

To describe a standardized method for measuring and comparing the viscosity of elixir formulations between production batches using a Brookfield viscometer or equivalent instrument to ensure consistency and product quality.

2. Scope

This SOP applies to the Quality Control Department for in-process and final product testing of viscosity in all batches of elixir formulations. It also supports trend analysis and investigation of process variability.

3. Responsibilities

  • QC Analyst:
    • Perform viscosity measurements and record data as per test method.
  • QC Supervisor:
    • Review results, verify consistency between batches, and identify outliers.
  • QA Officer:
    • Ensure that batch release is aligned with viscosity specifications.
See also  Elixir Department: SOP for Operation of Transfer Pumps - V 2.0

4. Accountability

The QC Head is accountable for conducting viscosity testing as per the defined method. The QA Head is responsible for monitoring batch consistency and approving product release based on viscosity results.

5. Procedure

5.1 Equipment and Materials

  • Brookfield viscometer with appropriate spindle set (e.g., LV series)
  • Beakers (100 mL/250 mL)
  • Thermometer (calibrated)
  • Water bath (to maintain sample at 25°C ± 0.5°C)

5.2 Sample Preparation

  1. Withdraw approximately 100 mL of the elixir sample.
  2. Bring the sample to 25°C using a calibrated water bath.
  3. Mix gently to ensure uniformity without introducing air bubbles.

5.3 Instrument Setup

  1. Ensure the viscometer is calibrated and on a vibration-free surface.
  2. Select the appropriate spindle (e.g., spindle #1 or #2) based on expected viscosity range.
  3. Set the rotation speed as per method validation (e.g., 30 rpm).
See also  Elixir Department: SOP for Addition of Volatile Solvents Under Fume Hood - V 2.0

5.4 Viscosity Measurement

  1. Immerse the spindle into the sample to the immersion mark.
  2. Start the viscometer and allow reading to stabilize for 30–60 seconds.
  3. Record the viscosity in centipoise (cP).
  4. Repeat the measurement in triplicate and calculate the average.

5.5 Batch Comparison

  1. Compare current batch viscosity with previous 3–5 consecutive batches.
  2. If variation is more than ±10% of historical average, investigate for root cause (e.g., ingredient concentration, temperature fluctuation, process deviation).

5.6 Acceptance Criteria

  1. Viscosity should be within specified range for the formulation (e.g., 300–600 cP).
  2. Trend should remain consistent with previous batches unless justified.

5.7 Documentation

  1. Enter results in the Viscosity Comparison Logbook (Annexure-1).
  2. Attach instrument printouts or screenshots (if applicable).
  3. Include observations in the Batch Manufacturing Record (BMR).

6. Abbreviations

  • SOP: Standard Operating Procedure
  • QC: Quality Control
  • QA: Quality Assurance
  • cP: Centipoise
  • BMR: Batch Manufacturing Record
See also  Elixir Department: SOP for Addition of Color Solutions - V 2.0

7. Documents

  1. Viscosity Comparison Logbook (Annexure-1)
  2. Instrument Calibration Log
  3. Batch Manufacturing Record (BMR)

8. References

  • USP General Chapter <911> – Viscosity
  • Ph. Eur. 2.2.10 – Viscosity – Capillary Method
  • 21 CFR Part 211.160 – Laboratory Controls

9. SOP Version

Version: 2.0

10. Approval Section

Prepared By Checked By Approved By
Signature
Date
Name
Designation
Department

11. Annexures

Annexure-1: Viscosity Comparison Logbook

Date Batch No. Spindle/Speed Measured Viscosity (cP) Average of Previous Batches (cP) Pass/Fail Tested By Verified By
11/04/2025 ELX-0425-044 #2/30 rpm 525 510 Pass Rajesh Kumar Sunita Reddy

Revision History:

Revision Date Revision No. Revision Details Reason for Revision Approved By
01/01/2024 1.0 Initial SOP Release New SOP Creation QA Head
11/04/2025 2.0 Included batch comparison criteria Process Monitoring Improvement QA Head
Elixers V 2.0 Tags:Elixir colorants, Elixir dosage form, Elixir filtration techniques, Elixir flavoring agents, Elixir formulation, Elixir GMP compliance, Elixir manufacturing process, Elixir manufacturing SOPs, Elixir packaging requirements, Elixir pharmacopoeial standards, Elixir preparation methods, Elixir preservatives, Elixir production equipment, Elixir quality control, Elixir regulatory guidelines, Elixir shelf life, Elixir stability testing, Elixir sterilization methods, Elixir storage conditions, Elixir sweetening agents, Elixir viscosity modifiers, Hydroalcoholic solutions, Medicated elixirs, Non-medicated elixirs, Pharmaceutical elixirs

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Standard Operating Procedures V 1.0

  • Aerosols
  • Analytical Method Development
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  • Raw Material Stores
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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
  • Gels V 2.0
  • Injectables V 2.0
  • Ointments V 2.0
  • Raw Material Warehouse V 2.0
  • Tablet Manufacturing V2.0

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