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Elixir Department: SOP for pH Adjustment Using Buffers – V 2.0

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Elixir Department: SOP for pH Adjustment Using Buffers – V 2.0

Standard Operating Procedure for pH Adjustment Using Buffers in Elixir Manufacturing

Department Elixir Department
SOP No. SOP/ELX/060/2025
Supersedes SOP/ELX/060/2022
Page No. Page 1 of 8
Issue Date 11/04/2025
Effective Date 15/04/2025
Review Date 11/04/2026

1. Purpose

To outline the procedure for adjusting and maintaining the pH of elixir formulations using appropriate buffer solutions to ensure product stability and efficacy.

2. Scope

This SOP applies to all elixir batches in the Elixir Department where pH adjustment is required during or after mixing, prior to filtration or filling.

3. Responsibilities

  • Manufacturing Operator:
    • Prepare and add buffer solutions as per batch instructions.
    • Perform in-process pH measurement and record values.
  • Production Supervisor:
    • Verify pH range compliance and authorize pH correction steps.
  • QA Officer:
    • Cross-verify final pH values and ensure SOP compliance.

4. Accountability

The Production Head is accountable for ensuring pH is maintained within specified limits for each batch and all adjustments are documented and verified.

See also  Elixir Department: SOP for Mixing and Homogenization of Elixir Components - V 2.0

5. Procedure

5.1 Pre-Check for pH

  1. Stop mixing and allow batch to stabilize for 5–10 minutes
before sampling.
  • Using a calibrated pH meter, take samples from the top, middle, and bottom of the tank.
  • Record pH values and compare them with batch specifications (as per BMR).
  • 5.2 Buffer Preparation

    1. Prepare buffer solutions using pharmaceutical-grade materials (e.g., citric acid, sodium citrate, sodium acetate, acetic acid).
    2. Dissolve measured quantity of buffer in purified water using clean glassware.
    3. Label each prepared buffer with:
      • Name of buffer
      • Concentration
      • Prepared on and used by dates

    5.3 pH Adjustment

    1. If pH is lower than specified, add alkaline buffer (e.g., sodium citrate).
    2. If pH is higher than specified, add acidic buffer (e.g., citric acid).
    3. Add buffer solution slowly under continuous stirring at moderate speed (50–80 RPM).
    4. After each addition, stir for 10 minutes and recheck the pH.
    5. Continue the process until the pH falls within acceptable range.

    5.4 Post-Adjustment Checks

    1. Perform final pH check from three points (top, middle, bottom).
    2. Document pH values in the pH Adjustment Log (Annexure-1).
    3. Get verification from Supervisor and QA before proceeding to the next manufacturing step.

    5.5 Meter Calibration

    1. Ensure the pH meter is calibrated with standard buffer solutions (pH 4.0, 7.0, and 10.0) before use.
    2. Enter calibration details in the pH Meter Calibration Log (Annexure-2).

    6. Abbreviations

    • SOP: Standard Operating Procedure
    • BMR: Batch Manufacturing Record
    • QA: Quality Assurance
    • pH: Potential of Hydrogen

    7. Documents

    1. pH Adjustment Log (Annexure-1)
    2. pH Meter Calibration Log (Annexure-2)
    3. Buffer Preparation Record (Annexure-3)

    8. References

    • USP General Chapter <781> pH
    • ICH Q6A – Specifications: Test Procedures and Acceptance Criteria
    • 21 CFR 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: pH Adjustment Log

    Date Batch No. Initial pH Buffer Used Final pH Adjusted By Verified By
    11/04/2025 ELX-1006 4.2 Sodium Citrate 4.8 Rajesh Kumar Sunita Reddy

    Annexure-2: pH Meter Calibration Log

    Date Instrument ID Buffer Used Calibrated By Verified By
    11/04/2025 PHM-03 pH 4.0, 7.0 Ajay Mehta Manju Sharma

    Annexure-3: Buffer Preparation Record

    Date Buffer Type Concentration Prepared By Used By
    11/04/2025 Citric Acid Buffer 0.1 M Rajesh Kumar 12/04/2025

    Revision History:

    Revision Date Revision No. Revision Details Reason for Revision Approved By
    01/01/2024 1.0 Initial SOP Release New SOP QA Head
    11/04/2025 2.0 Added Calibration and Multi-point Sampling Process Optimization 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
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    NEW! Revised SOPs – V 2.0

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