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.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callMore From: European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V
Paper Title
Journal
Date
