Formulation and Analytical Development for Low-Dose Oral Drug Products
Regular price
€134.99
14 days return policy
Shipping & Delivery
analytical chemistry of low-dose oral drug products
Category=MKG
Category=TDCW
eq_bestseller
eq_isMigrated=1
eq_nobargain
eq_non-fiction
eq_tech-engineering
formulation of low-dose drugs
formulation of low-dose oral drug products
Jack Zheng
low-dose drugs
low-dose oral drug products
manufacture of low-dose drugs
manufacture of low-dose oral drug products
regulation of low-dose drugs
regulation of low-dose oral drug products
Zheng
Product details
- ISBN 9780470056097
- Weight: 798g
- Dimensions: 163 x 243mm
- Publication Date: 10 Mar 2009
- Publisher: John Wiley & Sons Inc
- Publication City/Country: US
- Product Form: Hardback
Secure
checkout
Fast Shipping
Easy returns
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, Raman microscopy, and LC-MS and presents manufacturing techniques such as granulation, compaction, and compression. Complete with case studies and a discussion of regulatory requirements, this is a core reference for pharmaceutical scientists, regulators, and graduate students.
Jack Zheng, PhD, is Research Advisor and Team Leader in the Pharmaceutical Sciences R&D Division of Eli Lilly and Company and Adjunct Professor at Beijing University. Dr. Zheng is the author of more than thirty articles and several book chapters. He has been invited to present his work at numerous national and international scientific meetings. He was involved in more than ten new drug product development and regulatory filing with the Food and Drug Administration.
