Author:
Chaturvedi Kaushalendra,Shah Harsh S.,Sardhara Rusha,Nahar Kajal,Dave Rutesh H.,Morris Kenneth R.
Subject
Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry
Reference30 articles.
1. FIP/AAPS guidelines to dissolution/in vitro release testing of novel/special dosage forms;Siewert;AAPS PharmSciTech,2003
2. Guidance for industry--immediate-Release solid oral dosage Forms/Scale-Up and postapproval changes: chemistry, manufacturing, and controls; in vitro dissolution testing; in vivo bioequivalence;Rudman;Pharma. Technol.,1996
3. G.C. USP, 1092 The Dissolution Procedure Development and Validation, USP 34-NF 29 (2011).
4. Advances in pharmaceutical materials and processing;Morris;Pharm. Sci. Technol. Today,1998
5. Achieving continuous manufacturing: technologies and approaches for synthesis, workup, and isolation of drug substance. May 20–21, 2014 Continuous Manufacturing Symposium;Baxendale;J. Pharm. Sci.,2015
Cited by
6 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献