Analytical method development in the pharmaceutical industry is the systematic process of designing procedures to reliably identify, separate, and quantify […]
Analytical Method Development and Validation in Pharmaceuticals Read More »
In today’s fast moving pharmaceutical field, Peptide Testing Services are very important for making sure therapeutic efficacy, safety, and regulatory
Introduction NDSRI impurity synthesis has emerged as a critical area of focus in pharmaceutical impurity profiling and regulatory compliance. Nitrosamine
Introduction: Why NDSRI Impurity Analysis Method for Pharmaceuticals Matters Today The detection and control of Nitrosamine Drug Substance-Related Impurities (NDSRIs)
NDSRI Impurity Analysis in Pharmaceuticals: FDA & EMA Regulatory Requirements Read More »
Introduction: Why Nitrosamine Analysis for Over-the-Counter Drug Products Is Crucial The presence of nitrosamines—classified as probable human carcinogens—has raised significant
How to Test OTC Drug Products for Nitrosamines: LC-MS/MS vs. GC-MS Methods Compared Read More »
Introduction: Why Characterization of Peptides for FDA Matters The characterization of peptides for FDA approval is a very important part
When it comes to pharmaceutical and biopharmaceutical development, ensuring the safety of your product isn’t just about the drug itself—it’s
Key Analytical Techniques in E&L Testing Read More »
Introduction Over the past few years, Nitrosamine Testing for API Manufacturers in Canada has moved from being a regulatory formality
Nitrosamine Testing for API Manufacturers in Canada: Why It’s Non-Negotiable Read More »
Introduction Polymers form the molecular backbone of countless advanced materials that shape our world – from life-saving medical implants to
When you’re creating something that depends on polymers — whether it’s a medical device, a flexible film, or a high-performance
The Role of Polymer Analysis in Quality Control Read More »
