Real World Evidence
Meet your clinical, economic, and regulatory needs throughout a product's lifecycle
Systematic literature reviews of submissions to EMA, FDA, and HTA bodies can help overcome operational and methodological hurdles and mitigate regulatory risk. While FDA and EMA online databases facilitate document retrieval, acquiring key documents from disparate HTA bodies can be complex.
Read this case study to learn how IQVIA's platforms and capabilities, including Natural Language Processing (NLP) and Instant Translation Platform enables a side-by-side comparison of regulatory and HTA feedback, leading to actionable insights and significant time-savings.
Meet your clinical, economic, and regulatory needs throughout a product's lifecycle