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 Calibration of Measuring Instruments

Posted on By

SOP for Calibration of Measuring Instruments

Standard Operating Procedure for Calibration of Measuring Instruments

1) Purpose

The purpose of this SOP is to establish procedures for the calibration of measuring instruments used in the manufacturing of dental dosage forms, ensuring that all instruments provide accurate and reliable measurements necessary for maintaining product quality and regulatory compliance.

2) Scope

This SOP applies to all measuring instruments used in the production, testing, and control of dental pastes, gels, and mouthwashes within the pharmaceutical industry, including but not limited to scales, thermometers, pH meters, and pressure gauges.

3) Responsibilities

The Quality Assurance (QA) Department is responsible for overseeing the calibration program. The Engineering Department is responsible for performing calibrations and maintaining calibration records. All personnel using measuring instruments are responsible for ensuring instruments are within their calibration period before use.

See also  SOP for Cleaning and Sanitization of Packaging Equipment

4) Procedure

4.1 Identification of Instruments for Calibration

4.1.1 Compile a list of all measuring instruments requiring calibration, including details such as instrument type, manufacturer, model, serial number, and location.

4.1.2 Assign a unique identification number to each instrument for tracking purposes.

4.2 Calibration Schedule

4.2.1 Develop a calibration schedule based on the criticality of measurements, manufacturer’s recommendations, regulatory requirements, and historical calibration data.

4.2.2 Ensure that all instruments are calibrated at appropriate intervals and maintain an

up-to-date calibration schedule.

4.3 Calibration Procedures

4.3.1 Follow manufacturer’s instructions and approved calibration procedures for each type of instrument, using certified reference standards and equipment.

See also  SOP for Paste Manufacturing Equipment

4.3.2 Document calibration results, including the date of calibration, reference standards used, calibration readings, and any adjustments made.

4.3.3 Affix calibration status labels to instruments, indicating the date of calibration and the due date for the next calibration.

4.4 Handling Out-of-Tolerance Instruments

4.4.1 Identify any instruments found to be out of tolerance during calibration and remove them from service immediately.

4.4.2 Investigate and document the impact of using out-of-tolerance instruments on product quality and take appropriate corrective actions.

4.4.3 Recalibrate or replace out-of-tolerance instruments before returning them to service.

4.5 Record-Keeping and Documentation

4.5.1 Maintain comprehensive calibration records for each instrument, including calibration certificates, calibration logs, and records of any adjustments or repairs.

See also  SOP for Audit and Inspection of Equipment

4.5.2 Store calibration records in a manner that ensures easy retrieval for audits and inspections.

5) Abbreviations, if any

SOP – Standard Operating Procedure

QA – Quality Assurance

6) Documents, if any

Instrument Calibration Schedule

Calibration Procedures and Instructions

Calibration Certificates

Calibration Logs

7) Reference, if any

Manufacturer’s instructions for calibration

Regulatory guidelines for calibration of measuring instruments

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 Sterilization Tunnel
Next Post: SOP for Sealing Line for Gels

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