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Explore barriers to access in specific therapeutic areas including: oncology, infectious disease, orphan and rare diseases
Identify best practices for selecting and implementing specific treatment programmes for individual patients
Analyze the market uptake from previous launches that initiated an NPP prior to approval
Understand how to coordinate named patient programmes through the regulatory agencies at the macro and micro level
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Medical Affairs
Clinical Affairs/Operations
Market Access
Import/Export
Program Management
Global Business Development
Regulatory
Legal
Patient Services
Commercial Development
Global Communication
Marketing
Ethics
Research and Development
http://www.cbinet.com/show_conference.cfm?confCode=PC09075