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European Regulatory Procedures 2017
EMA has a 20-year track record of ensuring efficacy and safety of human and veterinary medicines across Europe, and promoting research and innovation in the development of medicines. In its first two decades, the Agency recommended the authorization of a total of 975 human and 188 veterinary medicines. EMA's success is based on cooperation within the European medicines regulatory network - a unique partnership between the European Commission,...
August 28-29, 2017
Organizer: GlobalCompliancePanel
Location: Opfikon-Glattbrugg, CH
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