Scott Cleve, VP of Regulatory Operations & Compliance at bluebird bio, discusses the following questions and more:

  • How did bluebird manage the rapid transition to remote work?
  • What changes have there been in interactions with FDA and other health authorities?
  • From a regulatory technology standpoint, what changes were needed to facilitate remote working?
  • In the new virtual world, how do you see inspection readiness changing?

You can also see the results from the study Scott references, Gens & Assoc. COVID-19 Regulatory Impact, here.

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