Gel Manufacturing: SOP for Calibration of Quality Control Instruments – V 2.0
Standard Operating Procedure for Calibration of Quality Control Instruments Used in Gel Manufacturing
| Department |
Gel Manufacturing |
| SOP No. |
SOP/GM/089/2025 |
| Supersedes |
SOP/GM/089/2022 |
| Page No. |
Page 1 of 12 |
| Issue Date |
02/06/2025 |
| Effective Date |
04/06/2025 |
| Review Date |
02/06/2026 |
1. Purpose
To establish a standardized procedure for the calibration of quality control (QC) instruments used in the gel manufacturing process, ensuring measurement accuracy, regulatory compliance, and consistent product quality.
2. Scope
This SOP applies to all quality control
instruments used for testing raw materials, in-process gels, and finished gel products in the Quality Control Laboratory associated with Gel Manufacturing.
3. Responsibilities
- QC Analyst: Performs calibration as per schedule and documents calibration results.
- QA Officer: Verifies calibration compliance and reviews documentation.
- QC Head: Approves calibration schedules and signs off calibration certificates.
- Engineering Department: Provides maintenance support and external calibration coordination.
4. Accountability
The Head – Quality Control is accountable for ensuring all instruments are calibrated according to the defined frequency and that the instruments are fit for intended use in gel product testing.
5. Procedure
5.1 Instrument Identification and Listing
- Maintain a comprehensive list of all QC instruments in the “Instrument Master List” (Annexure-1).
- Assign a unique instrument code to each device for traceability.
5.2 Calibration Planning
- Prepare an annual calibration schedule based on manufacturer’s recommendation, instrument usage, and criticality.
- Update the “Calibration Schedule Log” (Annexure-2) at the beginning of every calendar year.
5.3 Internal Calibration
- Perform internal calibration for instruments like:
- pH meters (using certified buffer solutions)
- Balances (using standard weights)
- Viscometers (using standard viscosity liquids)
- Record all results in the “Internal Calibration Record Sheet” (Annexure-3).
- Ensure results fall within predefined acceptance criteria. If not, escalate to QA.
5.4 External Calibration
- Coordinate with approved third-party vendors for calibration of instruments like:
- UV-Vis Spectrophotometer
- FTIR
- GC/HPLC (if applicable)
- Maintain calibration certificates in an indexed folder with cross-reference to Instrument ID.
- Log external calibration in the “External Calibration Summary” (Annexure-4).
5.5 Calibration Status Labeling
- Affix a “Calibration Label” to each instrument indicating:
- Instrument ID
- Date of Calibration
- Next Due Date
- Status: Calibrated / Out of Calibration
5.6 Handling Out-of-Calibration Instruments
- If calibration fails, label the instrument as “OUT OF CALIBRATION – DO NOT USE.”
- Initiate deviation report and investigate the impact on previous test results.
- Send the instrument for servicing or replacement as needed.
5.7 Review and Control
- QA reviews calibration records monthly.
- Audit readiness ensured through monthly checks and reconciliation of calibration certificates.
6. Abbreviations
- QC: Quality Control
- QA: Quality Assurance
- UV-Vis: Ultraviolet–Visible Spectroscopy
- FTIR: Fourier-Transform Infrared Spectroscopy
- GC: Gas Chromatography
- HPLC: High-Performance Liquid Chromatography
7. Documents
- Instrument Master List – Annexure-1
- Calibration Schedule Log – Annexure-2
- Internal Calibration Record Sheet – Annexure-3
- External Calibration Summary – Annexure-4
8. References
- ICH Q9: Quality Risk Management
- 21 CFR Part 211.68 – Automatic, Mechanical, and Electronic Equipment
- USP <1058> Analytical Instrument Qualification
9. SOP Version
Version: 2.0
10. Approval Section
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Prepared By |
Checked By |
Approved By |
| Signature |
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| Date |
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| Name |
|
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| Designation |
Jr. Production Chemist |
QA Executive |
Head – Manufacturing |
| Department |
Gel Manufacturing |
Quality Assurance |
Manufacturing |
11. Annexures
Annexure-1: Instrument Master List
| Sr. No. |
Instrument Name |
ID Code |
Location |
Calibration Frequency |
Status |
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Annexure-2: Calibration Schedule Log
| Month |
Instrument ID |
Instrument Name |
Scheduled Date |
Completion Date |
Done By |
Status |
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Annexure-3: Internal Calibration Record Sheet
| Date |
Instrument ID |
Standard Used |
Observed Value |
Acceptance Range |
Pass/Fail |
Remarks |
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Annexure-4: External Calibration Summary
| Calibration Date |
Instrument ID |
Service Provider |
Certificate No. |
Next Due Date |
Status |
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Revision History
| Revision Date |
Revision No. |
Change Description |
Reason |
Approved By |
| 01/06/2022 |
1.0 |
Initial Issue |
New SOP |
QA Head |
| 02/06/2025 |
2.0 |
Inclusion of external calibration log and annexure updates |
Periodic Review |
QA Head |