Autor: |
Susmitha, Aggarapu, Rajitha, Galla, Eri, Gireesh Kumar |
Předmět: |
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Zdroj: |
Journal of Liquid Chromatography & Related Technologies; 2023, Vol. 46 Issue 1-5, p12-36, 25p, 4 Diagrams, 15 Charts, 1 Graph |
Abstrakt: |
Quality has been a prime priority for the pharmaceutical sector with the development of recommendations by regulatory organizations like ICH. Concepts of ICH Q8 to Q10 are the foundation of the QbD methodology, a systematic approach to pharmaceutical development. Pharma industries have adopted the QbD approach to support product quality during manufacturing and to improve robust manufacturing processes. QbD adoption in analytical procedure development is AQbD, Analytical Quality by Design. It aids in reliable, economical analytical procedure development and also facilitates regulatory flexibility. This review illustrates the detailed aspects with relevant examples in each step of AQbD and DoE techniques applied to various analytical techniques for analytical procedure development for the determination of medicinal compounds. The overview of techniques created using AQbD contributes to the direction in this field of study. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
Externí odkaz: |
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