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Elixir Department: SOP for Real-Time pH Monitoring – V 2.0

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Elixir Department: SOP for Real-Time pH Monitoring – V 2.0

Standard Operating Procedure for Real-Time pH Monitoring During Elixir Manufacturing

Department Elixir Department
SOP No. SOP/ELX/192/2025
Supersedes SOP/ELX/192/2022
Page No. Page 1 of 9
Issue Date 11/04/2025
Effective Date 15/04/2025
Review Date 11/04/2026

1. Purpose

To define the procedure for continuous and accurate monitoring of pH in real-time during elixir manufacturing using in-line or online pH probes to ensure batch consistency and regulatory compliance.

2. Scope

This SOP is applicable to all elixir manufacturing processes requiring pH monitoring using real-time systems including in-line probes and digital pH monitoring devices integrated into manufacturing vessels and transfer lines.

3. Responsibilities

  • Production Operator:
    • Operate and clean the real-time pH monitoring device and monitor displayed readings during processing.
  • Engineering:
    • Ensure proper installation, calibration, and maintenance of pH sensors and transmitters.
  • QA Officer:
    • Verify that real-time pH logs are reviewed and maintained for every batch.
See also  Elixir Department: SOP for Calibration of Temperature Probes - V 2.0

4. Accountability

The Production Head is accountable for implementation and compliance of this SOP. The QA Head is responsible for periodic review and GMP adherence. Engineering Head is responsible for system reliability and performance.

5. Procedure

5.1 Equipment and Setup

  1. Ensure installation of a calibrated and validated real-time pH sensor in the manufacturing vessel or transfer line.
  2. Connect pH sensor to the digital display panel or SCADA system for live data visualization.
  3. Confirm probe calibration using standard pH 4.0 and 7.0 buffer solutions before batch start.
  4. Document calibration results in the pH Probe Calibration Logbook.

5.2 Real-Time Monitoring During Manufacturing

  1. Start pH monitoring once the initial solution is formed and maintain throughout mixing and ingredient addition phases.
  2. Observe the pH display and ensure it remains within the specified range defined in the BMR.
  3. Take manual note of pH at critical stages:
    • Post active ingredient dissolution
    • Post buffer addition
    • Post final volume adjustment
  4. If deviation occurs, notify QA and adjust pH using approved buffers (e.g., citric acid, sodium citrate) under supervision.
See also  Elixir Department: SOP for Sampling of Raw Materials for Elixirs - V 2.0

5.3 Cleaning and Maintenance of pH Probes

  1. After each batch, remove and clean the pH sensor using purified water followed by mild detergent solution.
  2. Do not allow probe to dry — store it in pH 4.0 storage solution when not in use.
  3. Inspect for any cracks, discoloration, or damage. Replace damaged sensors as per SOP.

5.4 Documentation

  1. Enter real-time pH data in the Real-Time pH Monitoring Logbook (Annexure-1) or electronic batch record system.
  2. Include:
    • Batch No.
    • Date and Time
    • pH Value
    • Stage of Manufacturing
    • Operator Initials
  3. QA to review and sign off each completed pH log.

6. Abbreviations

  • SOP: Standard Operating Procedure
  • QA: Quality Assurance
  • SCADA: Supervisory Control and Data Acquisition
  • BMR: Batch Manufacturing Record
See also  Elixir Department: SOP for Transfer of Bulk Elixir to Storage Tank - V 2.0

7. Documents

  1. Real-Time pH Monitoring Logbook (Annexure-1)
  2. pH Probe Calibration Log
  3. BMR Reference Sheet

8. References

  • ICH Q8 – Pharmaceutical Development
  • 21 CFR Part 211.110 – In-process Controls
  • WHO TRS 986 – GMP Guidelines

9. SOP Version

Version: 2.0

10. Approval Section

Prepared By Checked By Approved By
Signature
Date
Name
Designation
Department

11. Annexures

Annexure-1: Real-Time pH Monitoring Logbook

Date Batch No. Manufacturing Stage Observed pH Operator QA Review
11/04/2025 ELX-0425-011 Post Final Adjustment 6.8 Rajesh Kumar Sunita Reddy

Revision History:

Revision Date Revision No. Revision Details Reason for Revision Approved By
01/01/2024 1.0 Initial Release New SOP QA Head
11/04/2025 2.0 Included SCADA monitoring and calibration log 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
  • 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
  • Gels V 2.0
  • Injectables 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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