Pharma Conference and Expo
RMB 2,600Includes total access to 2-Day conference presentation and lunch
RMB 2,000Includes total access to 2-Day conference presentations and lunch
Adrian graduated in Pharmacy from the University of London after which he had a career of more than 35 years. He held senior positions in several functions, primarily in quality assurance overseeing manufacturing and supply operations. Currently, he works in an advisory capacity to IPEC Europe and the IPEC Federation, assisting these associations in their goals to exchange good practices and to develop harmonized standards for pharmaceutical excipients.
Priscilla is the current Chair of IPEC-Americas and has been a member of IPEC Americas committees since 2001 and a member of the IPEC Americas Executive Committee. She is also the Vice-President of the IPEC Federation. Priscilla has also participated for over 10 years in the International Food Additives Council and OFCA, a trade association for cellulose derivatives.
David R. Schoneker is the Director of Global Regulatory Affairs at Colorcon. His responsibilities include global coordination of Colorcon’s worldwide regulatory activities and market expansion projects to gain regulatory acceptance of Colorcon’s products and components for various target markets.
Susanne Keitel is a licensed pharmacist with a Ph.D. in pharmaceutical technology. Following ten years in the pharmaceutical industry, she held variatious senior positions at the Federal Institute for Drugs and Medical Devices (BfArM), Germany. Since October 2007, Susanne Keitel has held the post of Director of the European Directorate for the Quality of Medicine & HealthCare (EDQM), Council of Europe in Strasbourg.
Patricia has several years of experience in the pharmaceutical industry as a qualified person, quality manager, regulatory affairs, and involved in pharmaceutical development. She is active in a number of trade associations such as IPEC (International Pharmaceutical Excipient Council) since 1992, and is the current IPEC Federation President. Patricia contributed to numerous articles on pharmaceutical raw materials, and IPEC guidelines. She is a pivotal member of several excipient-related expert networks for Quality and Regulatory standards, including WHO. She is a member-elect of the French National Academy.
Ms. Skutnik is the Head of Quality Intelligence and Compendial Affairs at Biogen. In this role she is responsible for Review of regulations and guidances, globally that impact Biogen as well as many external engagement activities. Her former positions include: Vice President of Health Sciences at DBA, .Director /Team Leader of Quality & Regulatory Policy at Pfizer, responsible for working with various trade associations and also developing Pfizer Positions on Quality and CMC issues. She has over 20 years’ experience.
Gu Jingkai, Ph.D. in Pharmaceutical Analysis, Professor Tang Aoqing, Jilin University, PhD supervisor; Director of the Center for Drug Metabolism Research, Jilin University. Mainly engaged in drug and polymer materials analysis, pharmacokinetics and DMPK-based precursor drug design research work; concurrently Jilin University Molecular Key Laboratory of Ministry of Education Key Laboratory of Theoretical Chemistry.
He graduated from Ohio State University with Ph.D. in Pharmacy. In 2007, he worked at Abbott. He was appointed as a senior reviewer in the US Food and Drug Administration (FDA) Drug Test Center (CDER) in 2010. He was responsible for the approval of generic drugs, Liposomes and other complex pharmaceutical preparations CMC consistency evaluation and its cGMP quality system, and participated in the FDA's Nano Drug Administration Guidelines Expert Working Group, developed a number of liposome-related drug standards. Prior to serving the FDA, he was mainly engaged in the research of tumor drugs, monoclonal antibody drugs and nano-drug technology, and carried out cutting-edge work in the fields of liposome preparation, humanized antibody immunotherapy and siRNA delivery system.
Mr. Bill Dun, consultant of Beijing LFL technology company, providing consultancy, training and GMP audit service for pharmaceutical industry. He used to work for Merck, Millipore, IND pharmaceutical company, National serum and vaccine institute as compliance manager, validation manager, Chief engineer, QA manager and technician. He is also member of ISPE regulatory committee, expert of China national pharmaceutical packing association.