A Critical Review on Recently Used PAT in Pharmaceutical Industry
Author:
Affiliation:
1. Department of Pharmaceutical Sciences, School of Health Sciences and Technology, Dr. Vishwanath Karad MIT World Peace University, Sr.No. 124, MIT Campus Paud Road, Kothrud, Pune, Maharashtra 411038.
Abstract
Publisher
A and V Publications
Subject
Pharmacology (medical),Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
Reference38 articles.
1. Murphy T, O’ Mahony N, Panduru K, Riordan D, Walsh J. Pharmaceutical manufacturing and the quality by design (QBD), process analytical technology (PAT) approach. In 2016. p. 1–7.
2. Raj P, Gupta NV. Process analytical technology (PAT): A real time quality assurance. Int J Pharm Sci Rev Res. 2016 Jan 1;37:67–72.
3. Scott B, Wilcock A. Process Analytical Technology and Validation. In: Validation of Pharmaceutical Processes, Third Edition. 2007. p. 583–605.
4. Poozesh M, Ghasemzadeh H, Ablollahpour S, Diva MA. Effect of DL-Methionine Concentration, Moisture Content and Bulk Density of Animal Feed on the Light-Induced Fluorescence as a Process Analytical Tool. 2020;16.
5. Process Analytical Technology (PAT) in Pharmaceutical Development [Internet]. [cited 2021 May 14]. Available from: http://www.americanpharmaceuticalreview.com/Featured-Articles/115453-Process-Analytical-Technology-PAT-in-Pharmaceutical-Development/
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