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Clinical Development of Orphan Drugs

24 - 25 February 2015, London, United Kingdom


Introduction
A unique opportunity to build new relationships and improve existing partnerships between industry and patient organisations

Clarifying Regulations for Orphan Drugs with case-studies & recommendations to help you overcome common pitfalls in adhering to drug development regulations

Benchmark your orphan drug development programme against leading players such as Pfizer, GSK, Roche & NPS Pharma

Overcome challenges and gain solutions for small populations, critical considerations for trial design & strategies to boost patient enrollment & retention

Improve partnerships with patient organisations with critical recommendations for effective partnering

Get the most from your joint HTA/EMA meeting with critical insight and first-hand advice from NICE

Understand off-label use and its implications for product approval

Arrange one-to-one meetings with key stakeholders via EBD’s partnering system, groupsPLUS

Useful links

Venue
Park Plaza Victoria London

Park Plaza Victoria London, 239 Vauxhall Bridge Road, London, SW1V 1EQ, United Kingdom

Contact information
Rose Vincent
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