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

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

Creams: SOP for Calibrating Temperature Sensors in Manufacturing Equipment – V 2.0

Posted on By

Creams: SOP for Calibrating Temperature Sensors in Manufacturing Equipment – V 2.0

Standard Operating Procedure for Calibrating Temperature Sensors in Manufacturing Equipment

Department Creams
SOP No. SOP/CRM/084/2025
Supersedes SOP/CRM/084/2022
Page No. Page 1 of 5
Issue Date 21/01/2026
Effective Date 26/01/2026
Review Date 21/01/2027

1. Purpose

The purpose of this SOP is to outline the process for calibrating temperature sensors in manufacturing equipment. The objective is to ensure that temperature sensors are accurately measuring and controlling the temperature of materials during production, ensuring consistent product quality.

2. Scope

This SOP applies to the calibration of all temperature sensors in manufacturing equipment within the Creams Department, including those used in mixing, heating, cooling, and storage processes.

3. Responsibilities

  • Production Team: Responsible for following the calibration procedure and ensuring that temperature sensors are operating within the required specifications during production.
  • Maintenance Team: Responsible for calibrating the temperature sensors as per this SOP and ensuring they are in good working condition.
  • Quality Control (QC): Ensures that the calibrated temperature sensors are accurate and that product temperatures are within specified limits during production.

4. Accountability

The Head of Production is accountable for ensuring that temperature sensors are calibrated regularly and accurately. The QA Manager is responsible

for reviewing and ensuring the compliance of temperature control with quality standards.

See also  Creams: SOP for Analytical Testing of New Cream Formulations - V 2.0

5. Procedure

5.1 Pre-Calibration Checks

  1. Ensure that all temperature sensors to be calibrated are disconnected from the production line and are not currently in use.
  2. Verify that the calibration equipment, including a certified temperature reference standard (e.g., a calibrated thermometer or bath), is available and in good working condition.
  3. Ensure that the sensor calibration area is clean and free of any contaminants that could affect the calibration process.

5.2 Calibration Procedure

  1. Set the reference thermometer or bath to a known temperature that matches the expected operating temperature of the sensor being calibrated (e.g., 25°C, 50°C, or 100°C depending on the equipment requirements).
  2. Place the temperature sensor in the reference bath or attach it to the reference thermometer, ensuring that it is fully immersed and in good thermal contact.
  3. Allow the sensor to stabilize for a few minutes at the calibration temperature.
  4. Record the temperature displayed by the sensor and compare it with the reference temperature. If the readings match within the acceptable tolerance (typically ±1°C), the sensor is calibrated.
  5. If the sensor is out of tolerance, adjust the sensor’s output to match the reference temperature. Follow the manufacturer’s guidelines for adjusting the sensor, if applicable.
  6. Repeat the process for additional calibration points if required (e.g., at different temperatures or in different operational ranges).
See also  Creams: SOP for Setting Parameters for Planetary Mixers - V 2.0

5.3 Post-Calibration Checks

  1. After calibration, test the sensor again to ensure that it is consistently reading the correct temperature within the specified tolerance limits.
  2. Document the calibration results, including the reference temperature, sensor reading, tolerance, and any adjustments made in the Calibration Log (Annexure-1).
  3. Label the calibrated sensor with the calibration date and any relevant details (e.g., next calibration due date) for future reference.

5.4 Calibration Frequency

  1. Temperature sensors must be calibrated at regular intervals, typically once every six months, or more frequently if there are signs of malfunction or deviation in temperature readings.
  2. If any discrepancies are found during production, the sensor must be recalibrated or replaced immediately.

5.5 Documentation

  1. Ensure that all calibration records are documented in the Calibration Log (Annexure-1), including the date, sensor identification, calibration points, and any deviations or corrective actions taken.
  2. Record any issues found during calibration and corrective actions in the Temperature Sensor Maintenance Log (Annexure-2).

5.6 Final Approval

  1. The QA team must review all calibration documentation to ensure that temperature sensors are calibrated in accordance with GMP standards before the equipment is used in production.
  2. Upon approval, the sensor may be returned to production for use, ensuring that the temperature control system is fully operational.
See also  Creams: SOP for Material Transfer from Dispensing Area to Production Area - V 2.0

6. Abbreviations

  • GMP: Good Manufacturing Practices
  • QC: Quality Control
  • QA: Quality Assurance
  • PPE: Personal Protective Equipment
  • RTD: Resistance Temperature Detector

7. Documents

  1. Annexure-1: Calibration Log
  2. Annexure-2: Temperature Sensor Maintenance Log

8. References

  • Good Manufacturing Practices (GMP) Guidelines – 21 CFR Part 211
  • International Conference on Harmonisation (ICH) Q7 – Good Manufacturing Practice for Active Pharmaceutical Ingredients
  • ASTM E2877-13 – Standard Guide for Digital Contact Thermometers

9. SOP Version

Version: 2.0

10. Approval Section

Prepared By Checked By Approved By
Signature
Date
Name
Designation
Department

11. Annexures

Annexure-1: Calibration Log

Sensor ID Calibration Date Calibration Temperature Sensor Reading Tolerance Operator Comments
RTD-123 21/01/2026 25°C 25.1°C ±0.1°C John Doe Calibration successful

Annexure-2: Temperature Sensor Maintenance Log

Sensor ID Maintenance Date Issue Reported Corrective Action Operator Comments
RTD-123 21/01/2026 Deviation in reading Recalibrated sensor Jane Smith No further issues

Revision History:

Revision Date Revision No. Revision Details Reason for Revision Approved By
01/03/2024 1.0 Initial Version New SOP Creation QA Head
01/03/2025 2.0 Format Revision and Updates Standardization of Document QA Head
Creams V 2.0 Tags:Batch record documentation for creams, Change control procedures for cream manufacturing, Cleaning and sanitization SOPs in creams production, Complaint handling SOPs in creams production, Continuous improvement SOPs for cream manufacturing, Cream manufacturing process guidelines, Creams production documentation practices, Deviation handling SOPs in creams production, Employee training SOPs in creams manufacturing, Environmental monitoring SOPs in creams manufacturing, Equipment calibration SOPs for cream manufacturing, GMP compliance in creams production, Internal audit procedures in creams production, Packaging and labeling SOPs for creams, Pharmaceutical SOPs, Product quality review procedures for creams, Product release criteria SOPs for creams, Quality control SOPs for creams, ream manufacturing SOP, Regulatory requirements for cream production SOPs, Risk management SOPs in creams manufacturing, Stability testing SOPs for cream products, Standard operating procedures for skincare products, Supplier qualification SOPs for cream ingredients, Validation protocols for cream production processes

Post navigation

Previous Post: BA-BE Studies: SOP for Registration of BE Trials on CTRI – V 2.0
Next Post: Aerosol: SOP for Documentation of Packaging Operations – 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