[[Whitepaper]] Critical Considerations for Rare & Orphan Disease Trial Planning

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A question- first approach to Rare Disease Studies

Overcoming the unique challenges of rare A question- first approach to Rare Disease Studies disease drug development starts with asking the right questions. This paper is a guide to critical questions to ask and best practices to employ when developing and outsourcing rare disease clinical trials. Based on ARG’s decade of consulting around the world, this paper is designed to surface and mitigate the unique challenges rare disease studies present.

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In this whitepaper, we address:

  • Is your study protocol optimized for success in the intended population – and for the planned study sites?
  • Is your recruitment plan realistic? Could it be accelerated?
  • Are investigator sites adequately supported to ensure trial quality?

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This whitepaper was provided by Atlantic Research Group. Atlantic Research Group are sponsors of the upcoming World Orphan Drug Congress USA 2017 being held on April 20-21, 2017 in Washington D.C.Make sure to visit ARG at booth 314! To hear more from Atlantic Research Group and other Orphan Drug industry leaders, click here to register now >>

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