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

SOP for Temperature and Humidity Monitoring Equipment

Posted on By

SOP for Temperature and Humidity Monitoring Equipment

Standard Operating Procedure for Temperature and Humidity Monitoring Equipment

1) Purpose

The purpose of this SOP is to establish procedures for the calibration, operation, and maintenance of temperature and humidity monitoring equipment used in the manufacturing environment of dental dosage forms to ensure compliance with environmental control requirements.

2) Scope

This SOP applies to all temperature and humidity monitoring activities conducted in manufacturing areas producing dental pastes, gels, and mouthwashes within the pharmaceutical industry.

3) Responsibilities

The Facilities Management Department is responsible for executing temperature and humidity monitoring procedures. The Quality Assurance (QA) Department is responsible for verifying compliance with this SOP.

See also  SOP for Process Validation of Mouthwash Manufacturing

4) Procedure

4.1 Equipment Calibration

4.1.1 Calibrate temperature and humidity monitoring equipment regularly according to manufacturer’s specifications and calibration schedules.

4.1.2 Record calibration details including dates, results, and adjustments made.

4.2 Equipment Setup and Placement

4.2.1 Install temperature and humidity monitoring equipment in designated critical areas (e.g., manufacturing rooms, storage areas).

4.2.2 Ensure proper placement to accurately capture environmental conditions.

4.3 Monitoring Conditions

4.3.1 Monitor temperature and humidity levels continuously or at specified intervals as per regulatory requirements and operational needs.

4.3.2 Use validated monitoring devices to capture and record data effectively.

4.4 Alarm and Notification Systems

4.4.1 Set up alarm systems to alert personnel to temperature or humidity deviations

outside acceptable ranges.

See also  SOP for Tube Filling Machines

4.4.2 Document alarm events and corrective actions taken in response to deviations.

4.5 Data Recording and Reporting

4.5.1 Record temperature and humidity monitoring data accurately in designated logbooks or electronic systems.

4.5.2 Generate periodic reports summarizing monitoring results and trends.

4.6 Equipment Maintenance

4.6.1 Perform routine maintenance and cleaning of temperature and humidity monitoring equipment.

4.6.2 Replace sensors or components as needed to maintain equipment functionality.

5) Abbreviations, if any

SOP – Standard Operating Procedure

QA – Quality Assurance

6) Documents, if any

Calibration Certificates

Temperature and Humidity Monitoring Records

Alarm Logs

7) Reference, if any

Current Good Manufacturing Practices (cGMP) guidelines

See also  SOP for Cleaning and Sanitization of Filling Machines

International Conference on Harmonisation (ICH) guidelines for environmental control

8) SOP Version

Version 1.0

Dental Dosage Forms Tags:Audit and inspection of dental manufacturing, Calibration of dental equipment, Cleaning validation for dental products, Continuous improvement in dental production, Dental dosage form cleaning procedures, Dental dosage form equipment maintenance, Dental dosage form process validation, Dental Dosage Form SOPs, Dental dosage form validation procedures, Dental dosage forms manufacturing SOPs, Dental gel manufacturing guidelines, Environmental monitoring in dental manufacturing, Equipment qualification for dental dosage forms, Equipment qualification protocols dental, GMP compliance in dental manufacturing, Handling raw materials in dental manufacturing, Mouthwash manufacturing SOP, Packaging of dental products SOP, Quality control in dental dosage forms, Regulatory compliance in dental manufacturing, Risk assessment in dental manufacturing, Safety procedures for dental equipment, SOP for dental dosage form storage, SOP for dental paste production, SOP for dental product labeling, SOP for dental product manufacturing, Stability testing for dental products, Supplier qualification for dental equipment, Training documentation dental industry, Training programs for dental equipment, Validation master plan for dental equipment

Post navigation

Previous Post: SOP for Batch Release Procedures
Next Post: SOP for Automatic Eye Drop Filling Machine

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