Using IQVIA Integrated Solutions to Expedite a Systematic Literature Review and Inform Sponsor’s External Comparator Programs
Using IQVIA Integrated Solutions to Expedite a Systematic Literature Review and Inform Sponsor’s External Comparator Programs
2 PagesA biopharma sought to streamline real-world evidence for external comparators in regulatory and HTA submissions. IQVIA combined NLP with an Instant Translation Platform to analyze regulatory/HTA documents from FDA, EMA, NICE, G-BA/IQWiG, and HAS. The approach reduced review timelines by two months, preserved accuracy, and provided actionable insights into study design. Findings identified key success factors such as data quality, cohort comparability, endpoint selection, and sensitivity analyses. Results informed two publications in Clinical Pharmacology & Therapeutics.
