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 Determination of Moisture Content

Posted on By

Standard Operating Procedure for Moisture Content Determination in Manufacturing

 

Purpose

The purpose of this SOP is to outline the procedures for determining moisture content during the tablet manufacturing process to ensure product quality, stability, and compliance with regulatory requirements.

Scope

This SOP applies to all personnel involved in the tablet manufacturing process, particularly those responsible for moisture content determination.

Responsibilities

  • Quality Control Analysts: Responsible for conducting moisture content determination according to this SOP.
  • Production Department: Providing samples for testing and cooperating with quality control personnel.
  • Quality Assurance Department: Ensuring compliance with regulatory standards and guidelines.
See also  SOP for Tablet Dissolution Testing

Procedure

  1. Collect representative samples of tablets from the manufacturing process.
  2. Weigh and record the initial weight of the samples.
  3. Dry the samples using a suitable method such as oven drying or Karl Fischer titration.
  4. Weigh the dried samples and calculate the moisture content using the appropriate formula.
  5. Compare the moisture content results with established acceptance criteria.
  6. Document all testing procedures, observations, and results accurately and comprehensively.
  7. Review and approve the test results by authorized personnel.
  8. Take corrective actions if deviations from acceptance criteria are identified.

Abbreviations Used

SOP: Standard Operating Procedure
QC: Quality Control
QA: Quality Assurance

Documents

  • Moisture Content Determination Testing Protocol
  • Standard Operating Procedures Manual
  • Batch Records
  • Quality Control Reports
  • Deviation Reports
See also  SOP for Nebulizer Solution Performance Testing

Reference

No specific references are cited for this SOP.

SOP Version

Version 1.0

In-Process Control Tags:Antioxidant Testing, Appearance Inspection, Assay Testing, Batch testing, Blend Homogeneity Testing, Blend Uniformity Testing, Clarity Testing, Coating Thickness Measurement, Compliance testing, Container Closure Integrity Testing, Content Uniformity Testing, Disintegration Testing, Dissolution Profile Analysis, Dissolution Testing, Endotoxin testing, Friability Testing, Granule Size Distribution Analysis, Hardness Testing, In-process control, Leakage Testing, Manufacturing standards, Microbial Testing, Moisture Content Determination, Osmolality Testing, Particle Size Distribution Analysis, pH Testing, Process validation, Quality Assurance, Quality Control, Real-time monitoring, Sterility testing, Uniformity of Dosage Units Testing, Viscosity Testing, Weight Variation Testing

Post navigation

Previous Post: SOP for Incident Investigation and Reporting in Microbiology Lab
Next Post: SOP for In-Process Friability Testing

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