Biserka Cetina-Čižmek, PLIVA, Croatia
Biserka has been working in GR&D PLIVA pharmaceutical company in Croatia, member of Teva group for last twelve years. Her current position is Senior Director and head of Preformulation Department. She is pharmacist by education. She finished Ph.D. in Pharmaceutical Sciencie and worked as Senior Lecturer in field Pharmaceutical Analysis and since 2007 she has become Professor in the field of Pharmaceutical sciences at Faculty of Pharmacy and Biochemistry University of Zagreb. Her scientific background is the field of preformulation studies in drug development of solid dosage forms, semisolid and liquid, development of in vitro methodology to predict in vivo drug behavior, IVIV correlation, characterization of drug molecules, and BCS classification. She is author and co-author of 30 scientific papers, 47 posters and 12 oral presentations, 3 patent applications and mentor of 22 graduated and 3 postgraduate students.

Jasna Padovan, Fidelta d.o.o, Croatia
Jasna Padovan is Head of DMPK in Fidelta. She obtained a degree in biochemistry from the University of Colorado, was trained in PK/PD within the Leiden/Amsterdam Centre for Drug Research and obtained her PhD in Analytical Chemistry from the University of Zagreb. Jasna started her industrial career in 1998 working in the pharmaceutical and biotech companies PLIVA, GlaxoSmithKline and Galapagos mainly in the areas of anti-infectives, anti-fungals, inflammation and CNS, holding the position of head of DMPK. During her career she has worked on projects which have delivered seven development candidates. She has over 17 years of experience in the pharmaceutical industry, has over 10 scientific publications and has presented at several international conferences.
Christos Reppas, University of Athens, Greece
Christos is Professor of Pharmaceutics, Faculty of Pharmacy, National and Kapodistrian (N&K) University of Athens, Greece. He received his B. Pharm degree in Pharmacy from the N&K University in Athens in 1982 and his Ph.D in 1986 from the same University. From 1988 to 1989 he completed a postdoctoral fellowship in Pharmaceutics at the University of Michigan (USA) and then he joined the N&K University of Athens in 1989 as a Lecturer. He has held research positions with the University of London (UK), the University of Michigan (USA), Glaxo R&D (UK) and the University of Frankfurt (Germany). Research interests focus on the effects of gastrointestinal physiology on intralumenal performance of xenobiotics and the development of in vitro tests that are predictive of the intralumenal dosage form and drug performance. He is coauthor of more than 95 peer reviewed papers in international journals, two books and one patent.
Abu Serajuddin, St. John's University, New York, USA
Abu Serajuddin, Ph.D., is Professor of Industrial Pharmacy in the College of Pharmacy and Health Sciences at St. John’s University, Queens, New York, USA. He joined academia in 2008 after working for three decades in the pharmaceutical industry, where he formulated and developed numerous products, many with extremely difficult and challenging development issues. Several products that he developed or co-developed attained blockbuster status in the market. In his latest positions in the industry, Dr. Serajuddin served as the Director/Executive Director and the US Head of Drug Product Development (1999-2003) and Executive Director of Science, Technology and Outsourcing (2003-2008) for Novartis Pharmaceuticals Corporation. He authored over 90 research papers and book chapters and made over 100 invited presentations in scientific conferences. He is also a co-inventor in 12 patents. In recognition of his scientific and professional contributions, Dr. Serajuddin attained Fellow status in American Association of Pharmaceutical Scientists (AAPS), American Pharmacists Association (APhA), International Union of Pure and Applied Chemistry (IUPAC), and American Association of Indian Pharmaceutical Scientists (AAiPS). AAPS also honored him twice with its Research Achievement Award, first for Formulation Design and Development (FDD) in 2010 and the second for Manufacturing Sciences and Engineering (MSE) in 2014. In 2005, he received the Novartis Leading Scientist Award for extraordinary scientific achievement in research and development. He serves in the Editorial Advisory Boards of several journals, including Journal of Pharmaceutical Sciences. At St. John’s, Dr. Serajuddin established the Industrial Pharmacy Innovation Laboratory, where the primary focuses of his research are (1) the development of novel drug delivery systems, especially for poorly water-soluble drugs, and (2) the innovation in processing technologies for solid dosage forms.
Kin Tam, University of Macau, Macau
Kin Tam holds a DPhil in Physical Chemistry from the University of Oxford, UK. He is currently Associate Professor in Biomedical Sciences of the Faculty of Health Sciences, University of Macau, China. Before moving back to China in 2013, he worked for AstraZeneca, Alderley Park, UK, for 12 years, progressing from Senior Scientist, to Associate Principal Scientist, and working as a DMPK Design Leader from 2011. He contributed to a number of drug discovery projects in the areas of oncology and led the development of high-throughput physicochemical assays. Prior to joining AstraZeneca, he developed new instruments with Sirius Analytical Instruments, UK, for 5 years and commercialised UV-based devices for pKa determination. His current research interests include permeability and physiochemical studies of drug molecules, drug metabolism and pharmacokinetics as well as drug development. He has authored or co-authored over 70 articles in peer review journals. Dr. Tam is a Fellow of the Royal Society of Chemistry. He is currently the Editor-in-chief for ADMET & DMPK.

Klara Valko, Biomimetic chromatography consultancy, UK
Klara obtained her PhD at School of Pharmacy, Semmerlweis University in Budapest. Since 1995 Klara has been working with the Physico-chemical Characterization Group at GlaxoWellcome and now GSK. Leaving GSK after 22 years of service, now she is director of Bio-Mimetic Chromatography Consultancy providing data analysis, biomimetic HPLC method set up and measurements, in vivo drug distribution modelling and various courses to pharmaceutical companies and manufacturers of analytical equipment. She developed several bio-mimetic binding measurements of discovery compounds, such as Human Serum Albumin Binding, Immobilized Artificial Membrane binding and Chromatographic Hydrophobicity Index, etc. She developed in silico models for these and several other ADME properties using QSAR-WB general model building tool. Klara supported over 20 neuroscience and respiratory programs in the lead optimization by building general and local models between structure and properties. Klara is also a honorary professor at University College London, where she has been teaching the Physchem/ADME module for the Drug Discovery MSc students for 10 years. She has published over 100 papers that achieved over 3000 citations. She wrote a book on “Physicochemical and Biomimetic Properties in Drug Discovery; Chromatographic Techniques for lead optimization” published by Wiley in 2014. The book summarizes the methodology and applications of the measurements of physicochemical and biomimetic properties with examples for in vivo distribution models and applications in drug discovery.