Rare Disease & Orphan Drug Development: Cost-Efficient Trial Design to Minimize Cash Burn

MessageThis Webinar is over
Date Jun 1, 2017
Time 10am BST (UK) / 11am CEST (EU-Central) / 5am EDT (NA)
Cost Free
Discussion topics include:
  • Key challenges to improve cost-efficiency in clinical development of orphan drugs
  • Regulatory evolution in the review process of Orphan Drugs
  • After examples like Sarepta's Exondys51 approval, how will the evaluation of clinical benefits change based on endpoints?


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