SOP Guide for Pharma

Analytical Method Development: SOP for Calibration of Analytical Balances – V 2.0

Analytical Method Development: SOP for Calibration of Analytical Balances – V 2.0

Standard Operating Procedure for Calibration of Analytical Balances in Analytical Method Development


Department Analytical Method Development
SOP No. SOP/AMD/386/2025
Supersedes SOP/AMD/386/2022
Page No. Page 1 of 12
Issue Date 01/06/2025
Effective Date 04/06/2025
Review Date 01/06/2027

1. Purpose

To establish a standardized procedure for the calibration of analytical balances used in the Analytical Method Development (AMD) department. This ensures the accuracy and precision of weight measurements used

in method development, validation, and routine analysis activities.

2. Scope

This SOP applies to all analytical balances installed and used in the AMD laboratories, including microbalances and top-loading balances, for routine weighing operations. It covers daily calibration checks, monthly verifications, and annual third-party calibration procedures.

3. Responsibilities

  • Analytical Chemist: Performs daily and monthly internal calibration checks and records observations.
  • Instrument Coordinator: Schedules annual calibration with an external certified agency and maintains calibration certificates.
  • Quality Assurance: Verifies calibration status and reviews calibration records during internal audits.

4. Accountability

The Head of AMD is accountable for ensuring all analytical balances are calibrated as per the schedule and used only within the calibration validity period to maintain GMP compliance and data integrity.

5. Procedure

5.1 Calibration Classification

  • Daily Calibration: Performed by the user with certified calibration weights before use each day.
  • Monthly Verification: Conducted by the Instrument Coordinator using internal SOP-defined limits.
  • Annual Calibration: Carried out by an external NABL-accredited agency with traceable standards.

5.2 Daily Calibration Procedure

  1. Switch ON the balance at least 30 minutes before use.
  2. Ensure the balance is clean and placed on a vibration-free surface.
  3. Use certified calibration weights (Annexure-1).
  4. Calibrate at three points: 10%, 50%, and 100% of balance capacity.
  5. Record actual readings and calculate percent deviation from standard weight.
  6. Acceptable deviation: ±0.1% of standard weight.
  7. If deviation exceeds limits, inform QA and stop using the balance until corrective action is taken.

5.3 Monthly Verification Procedure

  1. Perform same steps as daily calibration but include additional intermediate weight checks (e.g., 25%, 75%).
  2. Record results in the Monthly Balance Calibration Log (Annexure-2).
  3. Affix “Verified” label with date and initials.

5.4 Annual Calibration by External Agency

  1. Schedule calibration at least 15 days before the due date.
  2. Ensure agency is NABL-accredited and provides traceable calibration certificates.
  3. Maintain a master calibration file including:
    • Certificate of calibration
    • Weight traceability reports
    • Calibration curves if applicable
  4. Tag instrument with “Calibrated” sticker mentioning calibration date and due date.

5.5 Out-of-Tolerance (OOT) and Breakdown Management

  1. If balance fails calibration:
    • Label as “Out of Service.”
    • Log deviation in instrument OOT Register (Annexure-3).
    • Initiate root cause analysis and document CAPA plan.
  2. Balance may be recalibrated or repaired before being reinstated.

5.6 Documentation and Records

  1. Ensure calibration records are filled completely, signed, and dated.
  2. Preserve all logs for a minimum of 5 years or as per GMP document retention policy.
  3. QA must verify calibration status during audits and batch reviews.

6. Abbreviations

  • GMP: Good Manufacturing Practices
  • NABL: National Accreditation Board for Testing and Calibration Laboratories
  • OOT: Out of Tolerance
  • QA: Quality Assurance
  • SOP: Standard Operating Procedure

7. Documents

  1. Annexure-1: Daily Calibration Checklist
  2. Annexure-2: Monthly Calibration Log
  3. Annexure-3: OOT Deviation Register
  4. Annual Calibration Certificate File

8. References

  • 21 CFR Part 211.68 – Automatic, Mechanical, and Electronic Equipment
  • ICH Q10 – Pharmaceutical Quality System
  • NABL Guidelines for Calibration Laboratories

9. SOP Version

Version: 2.0

10. Approval Section

Prepared By Checked By Approved By
Signature
Date
Name Ananya Sharma Deepak Tiwari Dr. Harshita Goyal
Designation AMD Analyst QA Reviewer Head – Analytical Method Development
Department Analytical Method Development Quality Assurance Analytical Method Development

11. Annexures

Annexure-1: Daily Calibration Checklist

Date Weight Used Observed Value Deviation (%) Status Initials
01/06/2025 100 mg 100.02 mg +0.02 Pass AS

Annexure-2: Monthly Calibration Log

Date Instrument ID Weight Range Status Initials
31/05/2025 AMD-BAL-02 10 mg–200 g Verified DT

Annexure-3: OOT Deviation Register

OOT ID Date Description Action Taken Status
OOT-386-01 20/05/2025 100 mg deviation +0.3% Re-calibrated by service team Closed

Revision History

Revision Date Revision No. Details Reason Approved By
01/06/2025 2.0 Expanded sections on monthly and annual calibration Annual SOP Review Dr. Harshita Goyal
01/05/2022 1.0 Initial version New SOP QA Head
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