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