Learn how you can update knowledge and know-how, find fresh ideas, learn from the experiences of top-level pharmaceutical experts, and create networking contacts that will enable you to make a difference at your company.The key challenge clinical trial supply chain managers face in global distribution is to ensure that supplies arrive at trial sites on time and in good condition.Effective distribution requires an understanding of regulations in the country of origin as well as in trial countries, it also requires qualified suppliers and storage infrastructure, control of supply temperature and conditions for the duration of delivery. Regulatory support is a critical aspect of clinical trial supplydistribution, requiring the creation and monitoring ofessential documents, study initiation, and activities toensure a seamless supply of clinical materials. Another regulatory role is labeling management - ensuringadherence to the labeling requirements of different countries, and managing their translation.Fleming Europe invites you to its 2nd Annual Clinical Trials Supply Chain conference where you can update knowledge and know-how, find fresh ideas, learn from the experiences of top-level pharmaceutical experts, and create networking contacts.HOT TOPICS:Maximizing Supply Chain EfficiencyGDP Compliance in Clinical SuppliesClinical Supplies in Emerging MarketsTemperature-Controlled DistributionOne Label for Global SupplyApplications of IRT TechnologiesForecasting and Planning