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Understanding Evaporation in Pharmaceuticals
In the fast-evolving world of pharmaceutical manufacturing, the operation of evaporation is far more than simple solvent removal. It is a mission-critical, scientifically engineered transformation that directly determines product quality, therapeutic potency, and regulatory success. Achieving precise concentration through controlled evaporation is a cornerstone of product stability, bioavailability, shelf life, and successful downstream processing.
Akshay Gautam
Nov 1511 min read


WHO GMP vs Indian GMP: A Manufacturer’s Guide to GMP
the blog provide idea about Good Manufacturing Practices (GMP) are the foundation of quality in the pharmaceutical industry. They ensure that every medicine is consistently safe, effective, and of high quality. This commitment to excellence protects public health and builds trust in medicines worldwide.
Globally, the World Health Organization (WHO) provides comprehensive GMP guidelines. The most important ones are TRS 986 Annex 2 for general GMP and TRS 1044 Annex 2 for ster
Akshay Gautam
Oct 1813 min read
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