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There are unique challenges in the formulation, manufacture, analytical chemistry, and regulatory requirements of low-dose drugs. This book provides an overview of this specialized field and combines formulation, analytical, and regulatory aspects of low-dose development into a single reference book. It describes analytical methodologies like dissolution testing, solid state NMR,...
Hoboken, New Jersey: John Wiley & Sons, 2009
e20393924
eBooks Universitas Indonesia Library
