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

Tag: Capsule weight variation SOP

SOP for Tablet Disintegration Testing

Posted on By

SOP for Tablet Disintegration Testing Procedure for Tablet Disintegration Testing 1) Purpose The purpose of this SOP is to outline the procedure for testing the disintegration of tablets to ensure they dissolve completely within the specified time frame for effective drug release. 2) Scope This SOP applies to all tablet batches produced within the manufacturing…

Read More “SOP for Tablet Disintegration Testing” »

In-Process Control

SOP for Tablet Friability Testing

Posted on By

SOP for Tablet Friability Testing Procedure for Tablet Friability Testing 1) Purpose The purpose of this SOP is to outline the procedure for determining the friability of tablets to ensure they have adequate mechanical strength to withstand handling and transportation. 2) Scope This SOP applies to all tablet batches produced within the manufacturing facility. 3)…

Read More “SOP for Tablet Friability Testing” »

In-Process Control

SOP for Tablet Thickness Measurement

Posted on By

SOP for Tablet Thickness Measurement Procedure for Measuring Tablet Thickness 1) Purpose The purpose of this SOP is to outline the procedure for measuring the thickness of tablets to ensure uniformity and compliance with specified dimensions. 2) Scope This SOP applies to all tablet batches produced within the manufacturing facility. 3) Responsibilities Quality Control (QC)…

Read More “SOP for Tablet Thickness Measurement” »

In-Process Control

SOP for Tablet Hardness Testing

Posted on By

SOP for Tablet Hardness Testing Procedure for Tablet Hardness Testing 1) Purpose The purpose of this SOP is to outline the procedure for determining the hardness of tablets to ensure they meet the required mechanical strength for packaging, handling, and usage. 2) Scope This SOP applies to all tablet batches produced within the manufacturing facility….

Read More “SOP for Tablet Hardness Testing” »

In-Process Control

SOP for Tablet Weight Variation

Posted on By

SOP for Tablet Weight Variation Procedure for Tablet Weight Variation Testing 1) Purpose The purpose of this SOP is to outline the procedure for determining the weight variation of tablets to ensure uniformity and compliance with pharmacopeial standards. 2) Scope This SOP applies to all tablet batches produced within the manufacturing facility. 3) Responsibilities Quality…

Read More “SOP for Tablet Weight Variation” »

In-Process Control

SOP for Flowability Testing of Powders

Posted on By

SOP for Flowability Testing of Powders Procedure for Flowability Testing of Powders 1) Purpose The purpose of this SOP is to outline the procedure for determining the flowability of powders to ensure consistent and efficient handling during the manufacturing process. 2) Scope This SOP applies to all powder batches prepared for pharmaceutical production within the…

Read More “SOP for Flowability Testing of Powders” »

In-Process Control

SOP for Bulk Density and Tapped Density Testing

Posted on By

SOP for Bulk Density and Tapped Density Testing Procedure for Bulk and Tapped Density Analysis 1) Purpose The purpose of this SOP is to outline the procedure for determining the bulk density and tapped density of powders and granules to ensure consistency in the manufacturing process. 2) Scope This SOP applies to all powder and…

Read More “SOP for Bulk Density and Tapped Density Testing” »

In-Process Control

SOP for Moisture Content Determination in Granules

Posted on By

SOP for Moisture Content Determination in Granules Procedure for Determining Moisture Content in Granules 1) Purpose The purpose of this SOP is to outline the procedure for determining the moisture content in granules used in pharmaceutical manufacturing to ensure product stability and quality. 2) Scope This SOP applies to all granule batches prepared for tablet…

Read More “SOP for Moisture Content Determination in Granules” »

In-Process Control

SOP for Granulation Size Distribution

Posted on By

SOP for Granulation Size Distribution Procedure for Granulation Size Distribution Analysis 1) Purpose The purpose of this SOP is to outline the procedure for determining the size distribution of granules used in pharmaceutical manufacturing to ensure consistency and quality in the final product. 2) Scope This SOP applies to all granulation batches prepared for tablet…

Read More “SOP for Granulation Size Distribution” »

In-Process Control

SOP for Blend Uniformity Testing

Posted on By

SOP for Blend Uniformity Testing Procedure for Blend Uniformity Analysis 1) Purpose The purpose of this SOP is to outline the procedure for performing blend uniformity testing to ensure the homogeneity of pharmaceutical blends prior to tablet or capsule production. 2) Scope This SOP applies to all pharmaceutical blends prepared for tablet or capsule production…

Read More “SOP for Blend Uniformity Testing” »

In-Process Control

Posts pagination

Previous 1 … 9 10

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