Skip to content
  • Clinical Studies
  • Pharma GMP
  • Pharma Tips
  • Stability Studies
  • Pharma Books
  • Schedule M

SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

  • Home
  • Job Safety Analysis (JSA)
    • Oral Dosage Forms (Tablets & Capsules)
    • Oral Liquid Dosage Forms (Syrups, Elixirs, Suspensions, Emulsions)
    • Powder and Granule Dosage Forms
    • Topical Dosage Forms (Creams, Ointments, Gels, Lotions, Pastes)
    • Transdermal Dosage Forms (Patches)
  • Standard Test Procedures (STP)
  • SOP – Blog Post
  • Toggle search form

API Manufacturing: SOP for Conductivity Measurement in Process Solutions – V 2.0

Posted on By

API Manufacturing: SOP for Conductivity Measurement in Process Solutions – V 2.0

Standard Operating Procedure for Conductivity Measurement in Process Solutions in API Manufacturing

Department API Manufacturing
SOP No. SOP/API/084/2025
Supersedes SOP/API/084/2022
Page No. Page 1 of 10
Issue Date 13/04/2025
Effective Date 15/04/2025
Review Date 13/04/2026

1. Purpose

To describe a standardized method for measuring the conductivity of process solutions in API manufacturing to monitor ionic strength, validate cleaning processes, and ensure consistency in intermediate reactions and aqueous washings.

2. Scope

This SOP applies to conductivity checks performed during aqueous extractions, reaction monitoring, washing of intermediates, and equipment cleaning verification in the API manufacturing facility.

3. Responsibilities

  • Production Chemist/Operator: Collect and measure samples as per process instructions.
  • QC Analyst: Verify conductivity meter calibration and review results.
  • QA Officer: Audit logbooks and ensure compliance with procedural accuracy.
See also  API Manufacturing: SOP for Cleaning Validation Between Batches - V 2.0

4. Accountability

The Production Head is accountable for operational control. The QC Head is responsible for analytical accuracy and data integrity.

5. Procedure

5.1 Instrument Calibration

  1. Calibrate the conductivity meter using certified standard solutions (e.g., 84 µS/cm and 1413 µS/cm) as per manufacturer’s instructions.
  2. Document calibration readings in the Conductivity Meter Calibration Log (Annexure-1).
  3. Do not use equipment with expired calibration or with deviation in standard reading beyond ±2%.

5.2 Sample Collection

  1. Collect process solution in clean, dry, and inert beakers or flasks.
  2. If sampling from a reactor or tank, ensure sample represents bulk solution and not surface layer.
  3. Allow solution to cool if collected from hot reaction mass (not above 40°C unless validated).

5.3 Measurement Technique

  1. Rinse the conductivity probe with distilled water and pat dry with lint-free tissue.
  2. Insert the probe into the sample ensuring full immersion of electrodes.
  3. Allow the reading to stabilize (typically 30 seconds to 1 minute).
  4. Record the value in µS/cm or mS/cm along with temperature (if auto-compensated).
  5. Document the reading in the Conductivity Measurement Log (Annexure-2) and BMR.
See also  API Manufacturing: SOP for Collection and Segregation of Used Solvents - V 2.0

5.4 Acceptance Criteria and Interpretation

  1. Refer to the approved process or cleaning validation protocol for acceptance ranges (e.g., conductivity NMT 10 µS/cm for final rinse).
  2. If outside limit, notify QA and repeat measurement using fresh sample.
  3. Initiate deviation report if reading remains out of specification.

5.5 Post-Use Maintenance

  1. After use, rinse the probe thoroughly with distilled water and store in 3M KCl or as recommended.
  2. Turn off the instrument and cover the probe to avoid dust or drying.

6. Abbreviations

  • SOP: Standard Operating Procedure
  • QA: Quality Assurance
  • QC: Quality Control
  • BMR: Batch Manufacturing Record
  • µS/cm: Microsiemens per centimeter
  • mS/cm: Millisiemens per centimeter

7. Documents

  1. Conductivity Meter Calibration Log (Annexure-1)
  2. Conductivity Measurement Log (Annexure-2)
  3. Batch Manufacturing Record
See also  API Manufacturing: SOP for Work-Up Procedure After Reaction Completion - V 2.0

8. References

  • ICH Q2(R1) – Validation of Analytical Procedures
  • 21 CFR Part 211 – US FDA cGMP
  • WHO TRS 986 – Good Manufacturing Practices

9. SOP Version

Version: 2.0

10. Approval Section

Prepared By Checked By Approved By
Signature
Date
Name
Designation
Department

11. Annexures

Annexure-1: Conductivity Meter Calibration Log

Date Meter ID Standard Used Expected Value Observed Value Calibrated By Remarks
13/04/2025 CD-01 1413 µS/cm 1413 1410 Within range

Annexure-2: Conductivity Measurement Log

Date Batch No. Process Stage Conductivity (µS/cm) Temperature (°C) Measured By Remarks
13/04/2025 API-20250413 Post-Wash 8.7 28 Within limit

Revision History:

Revision Date Revision No. Details Reason Approved By
01/01/2022 1.0 Initial Release New Instrument Control SOP QA Head
13/04/2025 2.0 Added interpretation and deviation handling steps Audit Compliance QA Head
API Manufacturing V 2.0 Tags:API batch record, API BMR, API calibration, API centrifuge, API cleaning, API crystallization, API deviation, API documentation, API drying, API equipment cleaning, API filtration, API GMP compliance, API granulation, API hold time, API impurities, API line clearance, API manufacturing, API process, API quality control, API reactor, API sampling, API solvent handling, API validation, API waste disposal, API yield

Post navigation

Previous Post: Analytical Method Development: Change Control for Developed Methods – V 2.0
Next Post: BA-BE Studies: SOP for Maintaining Privacy and Confidentiality of Volunteers – V 2.0

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

Read SOPs in your Language:

 - 
Bengali
 - 
bn
English
 - 
en
Gujarati
 - 
gu
Hindi
 - 
hi
Malayalam
 - 
ml
Marathi
 - 
mr
Punjabi
 - 
pa
Tamil
 - 
ta
Telugu
 - 
te

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.

Copyright © 2025 SOP Guide for Pharma.

Powered by PressBook WordPress theme

Go to mobile version