Understanding Pharmaceutical Excipients
This simplified guide explains what pharmaceutical excipients are, their types, functions, and why excipient selection matters in formulation development.
Understanding Pharmaceutical Excipients Read More »
This simplified guide explains what pharmaceutical excipients are, their types, functions, and why excipient selection matters in formulation development.
Understanding Pharmaceutical Excipients Read More »
“Understand bulk density vs tap density with formulas, examples, and applications in pharmaceutical powder flow and quality control.”
Bulk Density vs Tap Density Read More »
This blog provides a clear overview of 21 CFR, its importance, and the key sections relevant to the pharmaceutical industry.
21 CFR Guidelines Explained Read More »
Major pharmaceutical regulatory agencies and explains their key responsibilities in protecting public health.
Major Regulatory Agencies in the Pharmaceutical Industry and Their Roles Read More »
why are buffers used in HPLC analysis?
This blog explains the role, importance, and benefits of buffers in HPLC, especially in pharmaceutical and analytical laboratories.
Buffers in HPLC: Why Are Buffers Essential in HPLC Analysis? Read More »
This blog explains the major types of chromatography used in the pharmaceutical industry, along with their working principles and practical applications.
Types of Chromatography in Pharmaceutical Analysis Read More »
Difference Between Assay, Purity, and Potency in Pharmaceuticals
Difference Between Assay, Purity, and Potency in Pharmaceuticals Read More »
Why do we use three batches for process validation? This blog explains the scientific, statistical, and regulatory reasoning behind using three batches—and why this practice remains widely accepted across the industry.
Why Are Three Batches Used for Process Validation in Pharmaceuticals? Read More »
In this blog, we explain the three commonly used grades of water in the pharmaceutical and analytical industry: Milli-Q Water, Purified Water (PW), and Water for Injection (WFI).
Different Grades of Water in the Pharmaceutical and Analytical Industry Read More »
In the pharmaceutical industry, OOS (Out of Specification) and OOT (Out of Trend) are critical quality terms used in quality control (QC), laboratory testing, and product release decisions. Understanding the difference between OOS and OOT is essential to ensure regulatory compliance, data integrity, and product quality.
OOS vs OOT in Pharmaceuticals: Key Differences, Examples, and Actions Read More »