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When the Sponsor of a clinical trial experienced an unexpected 6-week delay in the regulatory approval of their master label text, they needed a creative way to make up for lost time.

Download this case study to learn how the Fisher Clinical Services project team helped:

  • Expedite the QA process, providing same day / next day approvals
  • Streamline production jobs by working in parallel while anticipating and proactively avoiding time-intensive processes
  • Mitigate risk of customs delays