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Sep 18 2014 9:30AM - Sep 18 2014 5:00PM | Hotel Pullman Brussels Midi
Place Victor Horta 1
The European Medicines Regulatory system is well developed and has achieved many successes in bringing medicinal products to the market to the benefit of patients and their health.However it has been receiving criticism for not supporting true innovation enough, for being bureaucratic, and full of redundancies and inefficiencies, which impact timelines and development costs.What of this is true, what is not? What could be improved and what needs to be changed?This workshop, organised jointly by DIA and TOPRA, will address these important questions and bring an important contribution to the debate improving the regulation for the benefit of all stakeholders.
Registration to the meeting is available on TOPRA website.Register NOW!
The Escher Project: scientific evidence and dialogue on the development and regulation of medicines.The Escher Project initiates research and policy debate on the development, marketing authorization, reimbursement and use of medicines. Our goal is to facilitate patient access to medicines and innovative technologies that address public health needs.............................................................Registration fees
To be booked via TOPRA
Industry fee - GBP665.50 = GBP550.00 + GBP115.50 (21% BE VAT) Government fee - GBP332.75 = GBP275.00 + GBP57.75 (21% BE VAT) Academic fee - GBP332.75 = GBP275.00 + GBP 7.75 (21% BE VAT) Student fee - GBP114.95 = GBP95.00 + GBP19.95 (21% BE VAT)
TOPRA and DIA have blocked a limited number of rooms at the following hotel:
Hotel Pullman Brussels MidiPlace Victor Horta 11060 Brussels Belgium
Tel.: (+32)25289800 Fax: (+32)25289801Email: H7431-SB@accor.comReference Code (ESCHER14)
at the rate of: EUR 169 per single room (inclusive of breakfast and VAT, excluding of city tax)Important: The room rate is available until 15 August 2014 or until the group block is sold-out, whichever comes first
Registration QuestionsTOPRAPhone.: +44 (0) 20 7510 2560 email@example.com
Agenda and Event LogisticsDIA EMEATamara Kohler, Team LeaderPhone: +41 61 225 51 57Fax: +41 61 225 51 firstname.lastname@example.org
Senior Expert, European Drug and Regulatory and International AffairsFederal Institute for Drugs and Medical Devices (BfArM), Germany
Director of EscherTI Pharma, Netherlands
Project Leader, Exon ConsultancyThe Escher Project, Netherlands
Executive Director, Global Regulatory PolicyMSD (Europe) Inc., Belgium
Senior Director, Regulatory Affairs, Clinical Research ServicesPAREXEL International, United Kingdom
Associate Director, Regulatory Affairs (Liver Disease)Gilead Sciences International Ltd, United Kingdom