An emerging biopharma (EBP) company focusing on theranostic development partnered with IQVIA to help accelerate its market approval process. The company sought IQVIA's expertise to navigate the complexities of the regulatory landscape and FDA requirements for Phase 1 study design.
Discover how IQVIA's approach, combining advanced technology with expert insights, provided tailored strategies that supported the EBP in effectively navigating the approval process. Read the case study now.
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