Pharma Conference and Expo
RMB 2,800Includes total access to 2-Day conference presentation and lunch
RMB 2,200Includes 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.
Ms. Sheehan is currently the Senior Director of Science – Excipients at the United States Pharmacopeial Convention. She co-leads the Excipients Program Unit responsible for championing the development of global quality excipient standards and related programs, outreaching to stakeholders, partnering to improve awareness and advocating for adoption of up-to-date excipient quality standards and related regulations. She also supports USP’s collaborative efforts with other pharmacopeial bodies worldwide towards successful harmonization and update of excipient monograph specifications. Ms. Sheehan is active in AAPS and RAPS. Ms. Sheehan holds both an M.S. Regulatory Science degree and M.S. Molecular Biotechnology degree from The Johns Hopkins University, Baltimore, USA. She is a doctoral candidate at the University of Southern California’s School of Pharmacy, International Regulatory Science Program.
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.
Sabine Kopp is Group Lead of WHO’s Medicines Quality Assurance team. She was Secretary for the International Nonproprietary Names (INN) Programme, Programme Manager for the Quality Assurance and the Anticounterfeiting Programmes, Acting Secretary of the International Medical Products Anti-Counterfeiting Taskforce (IMPACT) and actively involved in the WHO Member State mechanism on substandard and falsified medical products. Sabine Kopp is Secretary of the WHO Expert Committee on Specifications for Pharmaceutical Preparations, coordinating WHO's activities related to international quality assurance guidelines, GXPs, specifications and regulatory guidance for medicines, from their development to the supply to patients.
Dr. Frank Milek is an industrial pharmacist and has been working in pharmaceutical excipients industry for more than 15 years, specialised in the field of supply chain and distribution. He is registered QP according to EU regulation and responsible at Aug. Hedinger GmbH & Co. KG for Quality, Regulatory Affairs and GMP.Frank is currently the Vice-Chair of IPEC Federation, as well as Chair of the IPEC Europe GDP Committee and an active member of the EXCiPACT association. In parallel, he also chairs the GTDP Committee in FECC (European Association of Chemical Distributors).