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Follow on Google News | Develop new Market Access models for Orphan Drugs and Receive Case Studies from MSD, Sanofi & GSKSMi's 21st annual European Pharmaceutical Pricing & Reimbursement conference will address the impact of Biosimilars and Orphan Drugs on P&R, Case Studies in Reforms, Purchasing Mechanisms and Working with Payers.
By: SMi Group Against this backdrop, SMi’s 21st annual European Pharmaceutical Pricing & Reimbursement conference, taking place on 5-6 October 2015 in London, will provide the ideal platform for payers and other decision makers from both public and private organisations, to benchmark with peers internationally and provide pharma companies with an invaluable insight into the decision making processes and approaches of vital stakeholders. The two-day conference programme will help further your understanding and enable you to develop best practice approaches to complex market access challenges, with the ultimate goal of encouraging innovation and improving patient access to novel and powerful medications though case studies presented by GSK, Sanofi, MSD and more who will be presenting at the two-day conference. Unique perspectives will be shared on: • Case studies assessing of the impact Biosimilars and Orphan Drugs on the the market with MSD and Quintiles • Tiered pricing options with a case study from GSK • Case studies in Reforms with Sanofi sharing their perspective • Evaluating new models for European reimbursement • Health Technology Assessment policies • Changes in UK P&R policy following the UK elections with presentations from industry bodies such as EMIG and the ABPI Developing new Market Access models for Orphan Drugs • Principal aspects of policy and practice associated with orphan drugs and treatments of rare disease • Perspectives for 2015 on new and emerging approaches for addressing patient access. • Are payers treating orphan drugs differently Janice Haigh, Practice Leader, Market Access, Quintiles The Impact of Biosimilars on the Market • Analysing the characteristics of biosimilars and the development of the EU’s biosimilars market • Exploring the likely impact of biosimilars on future pharmaceutical budgets based on different scenarios and models • Identifying opportunities and challenges for industry, patients and payers, as well as appropriate pricing and reimbursement options – sustainable competition as a realistic option? Alexander Roediger, Director of European Union Affairs, MSD To view the full speaker line-up and conference programme, visit http://www.smi- Plus, don't miss the half-day interactive post-conference workshop: HTA Uncovered Led by Anke Van Engen, Principal - Advisory Services & Janice Haigh, Practice Leader Market Access, Quintiles 8.30 – 12.30 | 7th October 2015, Holiday Inn Regents Park, London, UK End
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