For Registration and Full Info please contact Cristina C. Lungu cristinah (at) mondialresearchgroup (dot) comThe content of this course will assist pharmaceutical, biotechnology, and CRO researchers andmanagers in understanding the requirements for a well-designed and successful ADMET,PK/TK, and DM program that is conducted within a drug development logic plan and incompliance ICH guidelines. The various types of ADME, PK/TK, and DM studies, which includein vitro metabolism and delivery, appropriate use of in vitro and in vivo mechanistic toxicityassays and their relationship with regulatory toxicology, animal and human pharmacokinetics,protein binding, mass balance, tissue distribution, metabolite isolation and identification, andtoxicokinetic support, will be discussed. Case studies of well and poorly designed programs,study designs and potential results, with possible interpretations, from each of the study typeswill be presented.