| Literature DB >> 32565295 |
Liang Zhong1, Lele Gao1, Lian Li1, Hengchang Zang2.
Abstract
Quality is the lifeline for all pharmaceuticals. Process analytical technology (PAT), introduced by FDA in 2004, providing significant opportunities for improving pharmaceutical development, manufacturing, and quality assurance. Therefore, in this review various PAT tools were introduced for solid oral dosage manufacture quality monitor and control. Throughout this review, we would like to provide more information to both researchers and manufacturers in order to improve the drug quality.Keywords: Chemometrics; Critical quality attributes; Process analytical technologies; Process control; Solid oral dosage forms
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Year: 2020 PMID： 32565295 DOI： 10.1016/j.ejpb.2020.06.008
Source DB: PubMed Journal: Eur J Pharm Biopharm ISSN： 0939-6411 Impact factor: 5.571