Bookedited by Elizabeth Kwong.
Contents:
Lead identification/optimization / Dr. Mei Wong And Dr. Mark Mcallister
Oral drug formulation development in pharmaceutical lead selection stage / Shayne Cox Gad
Bridging end of discovery to regulatory filing : formulations for IND- and registration-enabling nonclinical studies / Evan A. Thackaberry
Planning the first clinical trials with clinical manufacturing organization (CMO) / Elizabeth Kwong and Caroline McGregor
Formulation strategies for high dose toxicology studies : case studies / Dennis H. Leung, Pierre Daublain, Mengwei Hu, Kung-I Feng
Formulation, analytical and regulatory strategies for first in human clinical trials / Lorenzo Capretto, Gerard Byrne, Sarah Trenfield, Lee Dowden, and Steven Booth.