Category: Sin categoría
Innovation in the development of semisolid pharmaceutical forms
The revolution of semisolid pharmaceutical formulations The evolution of semisolid pharmaceutical forms has marked a decisive advancement in the fields…
Analysis of genotoxic impurities in active pharmaceutical ingredients
Importance of controlling genotoxic impurities in drug safety Drug safety begins long before a product reaches patients. During the development,…
Microbiological analysis of non-sterile medicines
Importance, methods, and quality control in microbiological analysis Microbiological analysis of non-sterile medicines is a critical component of pharmaceutical quality…
The importance of routine analysis in pharmaceutical development
Why is routine analysis essential in modern pharmaceutical development? In an increasingly regulated and technologically advanced pharmaceutical environment, routine analysis…
How extractables and leachables studies improve the stability and safety of pharmaceutical products
How to optimize pharmaceutical development through extractables and leachables studies Pharmaceutical development optimization largely depends on the ability to evaluate…
New USP <661.2> Monograph: Requirements and Compliance for Pharmaceutical Plastic Packaging
The USP <661.2> monograph will come into effect on December 1, 2025, discover what it requires and how to comply…
Optimization and advanced control in lyophilization processes
How the personalization of lyophilization processes is transforming the pharmaceutical industry The pharmaceutical industry is undergoing a profound transformation driven…
Importance of In-Use Stability Testing in Pharmaceutical Development
In-use stability testing, an essential requirement in drug evaluation In-use stability testing is a fundamental process within the development and…
Pre-Stability Studies with Qualified Climatic Chambers
What are Pre-Stability Studies? Pre-stability studies are tests carried out during early stages of the development of a pharmaceutical, cosmetic,…
7 Things you should know about toxicological assessment in pharmaceutical process validation
Toxicological assessment in pharmaceutical process validation The development of medicines requires rigorous control to ensure that the products reaching patients…
