Blog – burnautomation

03 Jul 2026

Analytical Balance Weighing: Best Practices for Accurate Pharmaceutical Measurements

Introduction Accurate weighing is one of the most fundamental operations performed in pharmaceutical laboratories. Whether preparing analytical standards, compounding formulations, or conducting…

03 Jul 2026

Tapped Density Testing: A Critical Measurement for Powder Flow and Pharmaceutical Manufacturing

Introduction The manufacture of high-quality pharmaceutical products begins with understanding the physical properties of powders. Among the most important of these properties…

03 Jul 2026

Tablet Friability Testing: Ensuring Mechanical Integrity of Solid Oral Dosage Forms

Introduction Tablet friability testing is an essential quality control procedure used to evaluate the ability of compressed tablets to withstand the mechanical…

03 Jul 2026

Disintegration Testing: A Critical Quality Control Test for Solid Oral Dosage Forms

Introduction Disintegration testing is a fundamental quality control procedure used throughout the pharmaceutical industry to verify that tablets and capsules break apart…

03 Jul 2026

The Scott Volumeter: A Standardized Method for Determining Bulk Density of Pharmaceutical Powders

Introduction The flow and packing characteristics of pharmaceutical powders play a critical role in tablet compression, capsule filling, blending, and packaging operations.…

03 Jul 2026

Tablet Breaking Force Testing: Evaluating the Mechanical Strength of Pharmaceutical Tablets

Introduction Tablet breaking force testing is one of the most important physical quality control tests performed during the development and manufacture of…

03 Jul 2026

Angle of Repose: A Practical Guide to Powder Flow Characterization in Pharmaceutical Manufacturing

Executive Summary The Angle of Repose (AoR) is one of the most widely used methods for evaluating powder flow characteristics in pharmaceutical…