Move swiftly through IND/CTA and into the clinic 30% faster with a prospective plan and unprecedented continuity. Your asset is surrounded with a cross-functional team of experts and proven efficient processes that save you time and money.
Experience a collaborative, flexible approach to your clinical trial. Engage with an executive lead for the duration of your program. Gain insights from a devoted team with scientific, regulatory and therapeutic expertise in your indication.
Enjoy streamlined safety and esoteric testing with a biotech-dedicated study management team. Get trial-specific specimen collection kits, unmatched logistics support and access to scientific expertise.
Reach patients who will benefit most from your novel drug through the power of precision medicine. Go from pathway selection, biomarker development and validation to an informed regulatory and commercial strategy for your companion diagnostic.
Advance your nonclinical and clinical strategies, navigate regulatory requirements and identify the right approach with a Target Product Profile. Then, pave the way to commercial success with insights from early-stakeholder and market research.
Make more informed decisions with confidence by leveraging a global network of clinical pharmacology units and integrated development approach to manage study complexity and efficiently execute trials in healthy volunteers, patients and special populations.
Reduce study costs, speed time to market and increase patient recruitment with visibility into optimal sites and clusters of eligible participants. Enable improved enrollment and retention with proprietary patient diagnostic data, unrivaled site performance data and unique patient insights.