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Day 1 The World Orphan Drug Congress – Geneva
Authored by Karl Simpson
Posted in Orphan Drugs and Rare Diseases, Pharmaceutical business
Tagged Adaptive Licensing, clinical development, Clinical Trial Design, Corporate Development and Partnerships, EURORDIS, Geneva, HTA, IRDiRC, Market Access, Nyon, Orphan drugs, pricing and reimbursement, rare diseases, Shire HGT, Theresa Heggie, world orphan drug congress, world orphan drug congress 2012, Yann Le Cam
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