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

SOP for Proper Positioning of Thermometers and Hygrometers in Storage Areas – V 2.0

Posted on By

SOP for Proper Positioning of Thermometers and Hygrometers in Storage Areas – V 2.0

Standard Operating Procedure for Proper Positioning of Thermometers and Hygrometers in Storage Areas

Department Warehouse / Quality Assurance / Maintenance
SOP No. SOP/RM/159/2025
Supersedes SOP/RM/159/2022
Page No. Page 1 of 12
Issue Date 28/03/2025
Effective Date 04/04/2025
Review Date 28/03/2026

1. Purpose

This Standard Operating Procedure (SOP) outlines the correct procedures for the placement, monitoring, and maintenance of thermometers and hygrometers in storage areas to ensure accurate recording of temperature and humidity levels. Maintaining optimal environmental conditions is crucial for the integrity and quality of raw materials.

2. Scope

This SOP applies to all storage areas within the warehouse where raw materials are stored. It includes procedures for the positioning, calibration, and documentation of temperature and humidity monitoring devices.

3. Responsibilities

  • Warehouse Personnel: Ensure proper placement of thermometers and hygrometers and report any discrepancies or device malfunctions.
  • Warehouse Supervisor: Oversee the correct positioning and functioning of monitoring devices and ensure records are maintained.
  • Quality Assurance (QA): Conduct regular audits to verify the accuracy of environmental monitoring and approve calibration schedules.
  • Maintenance Team: Responsible for the calibration and maintenance of thermometers and hygrometers.
See also  SOP for Storage of Raw Materials in Compliance with GMP Guidelines - V 2.0

4. Accountability

The Warehouse Manager is accountable for ensuring proper environmental monitoring in storage areas. The QA Manager is responsible for verifying compliance through audits and documentation.

5. Procedure

5.1 Selection and Calibration of Monitoring Devices

  1. Device Selection:
    • Select calibrated thermometers and hygrometers that meet regulatory standards for accuracy and reliability.
    • Devices should have a calibration certificate and be traceable to national or international standards.
    • Document device selection in the Device Selection Log (Annexure-1).
  2. Calibration Schedule:
    • All monitoring devices must be calibrated biannually by the Maintenance Team or an external accredited calibration service.
    • Maintain calibration records in the Device Calibration Log (Annexure-2).

5.2 Positioning of Thermometers and Hygrometers

  1. General Positioning Guidelines:
    • Place thermometers and hygrometers at locations that represent the average environmental conditions of the storage area.
    • Avoid placing devices near doors, vents, windows, or direct sunlight to prevent false readings.
    • Document device positioning in the Device Positioning Log (Annexure-3).
  2. Specific Positioning for Different Storage Areas:
    • For temperature-sensitive materials, place additional devices at the front, middle, and rear of the storage area.
    • Ensure devices are positioned at the same height as stored materials to reflect accurate environmental conditions.
    • Document specific positioning strategies in the Storage Area Monitoring Plan (Annexure-4).
See also  SOP for Handling and Storing Raw Materials with Short Shelf Life - V 2.0

5.3 Monitoring and Documentation

  1. Daily Monitoring:
    • Warehouse personnel must record temperature and humidity readings twice daily, once in the morning and once in the evening.
    • Document readings in the Temperature and Humidity Log (Annexure-5).
  2. Deviation Management:
    • In case of deviations from acceptable ranges, immediately inform the Warehouse Supervisor and QA.
    • Record deviations and corrective actions in the Environmental Deviation Log (Annexure-6).

5.4 Maintenance of Monitoring Devices

  1. Routine Checks:
    • Inspect thermometers and hygrometers weekly for signs of damage or malfunction.
    • Clean devices regularly to prevent dust accumulation that may affect accuracy.
    • Document maintenance activities in the Device Maintenance Log (Annexure-7).
  2. Replacement of Faulty Devices:
    • Replace any faulty devices immediately to ensure continuous environmental monitoring.
    • Record replacements in the Device Replacement Log (Annexure-8).

6. Abbreviations

  • SOP: Standard Operating Procedure
  • GMP: Good Manufacturing Practice
  • QA: Quality Assurance
  • MSDS: Material Safety Data Sheet

7. Documents

  1. Device Selection Log (Annexure-1)
  2. Device Calibration Log (Annexure-2)
  3. Device Positioning Log (Annexure-3)
  4. Storage Area Monitoring Plan (Annexure-4)
  5. Temperature and Humidity Log (Annexure-5)
  6. Environmental Deviation Log (Annexure-6)
  7. Device Maintenance Log (Annexure-7)
  8. Device Replacement Log (Annexure-8)
See also  SOP for Storage of APIs Under Controlled Conditions - V 2.0

8. References

  • 21 CFR Part 211 – Current Good Manufacturing Practice for Finished Pharmaceuticals
  • WHO Guidelines on Good Manufacturing Practices for Pharmaceutical Products
  • ISO/IEC 17025: General Requirements for the Competence of Testing and Calibration Laboratories

9. SOP Version

Version: 2.0

10. Approval Section

Prepared By Checked By Approved By
Signature
Date
Name
Designation
Department

Annexure-1: Device Selection Log

Date Device Type Model Number Supplier Selected By
28/03/2025 Thermometer THR-500 ThermoTech Pvt. Ltd. Ravi Kumar
28/03/2025 Hygrometer HYG-200 EnviroSensors Ltd. Neha Verma

Annexure-2: Device Calibration Log

Date Device Type Model Number Calibration Status Calibrated By
28/03/2025 Thermometer THR-500 Calibrated Amit Joshi
28/03/2025 Hygrometer HYG-200 Calibrated Priya Singh

Annexure-3: Device Positioning Log

Date Device Type Location Positioned By
28/03/2025 Thermometer Middle of Storage Room A Ravi Kumar
28/03/2025 Hygrometer Rear of Storage Room B Neha Verma

Revision History:

Revision Date Revision No. Revision Details Reason for Revision Approved By
01/01/2024 1.0 Initial Version New SOP Implementation QA Head
28/03/2025 2.0 Added Maintenance and Deviation Procedures Enhance Environmental Monitoring Accuracy QA Head
Raw Material Warehouse V 2.0 Tags:Audit compliance in material storage, Contamination prevention in warehouses, Documentation in warehouse operations, Emergency procedures in warehouses, Equipment maintenance in warehouses, FIFO method in inventory, Handling of hazardous materials, Inventory management SOP, Labeling requirements in warehouses, Loading and unloading procedures, Material inspection protocol, Material receiving process, Material segregation guidelines, Pest control in storage areas, Quality control in warehousing, Raw material handling SOP, Return material handling SOP, Safety procedures for material handling, Security measures for stored materials, Spill response procedures, Storage conditions for raw materials, Temperature and humidity control in storage, Training for warehouse personnel, Warehouse storage procedures, Waste management in warehouses

Post navigation

Previous Post: Ointments: SOP for Developing Ointments for Specific Skin Conditions – V 2.0
Next Post: Capsule: SOP for Validation of Cleaning Procedures for Capsule Polishing Machines – 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