Leverage powerful clinical development capabilities marked by quality, service, and value We deliver outstanding quality by recruiting the industry’s top talent and continuously improving our performance through training, operational excellence programs, and powerful technologies that produce increasingly refined results. We provide exceptional service because we’re customer-driven, focused on meeting timelines and staying in budget, addressing challenges proactively, communicating transparently, and going to great lengths to be easy to work with. And we offer extraordinary value, not by being the least costly, but by serving as one of your most trustworthy partners, consistently delivering results you can rely on—thanks to clinical development capabilities that include: Therapeutic Specialization Our specialization in five core areas—central nervous system, oncology, endocrinology and metabolic disease, respiratory and infectious disease and cardiology, helps you meaningfully improve patient care. We design and implement customized, state-of-the-art rater training programs that can enhance the validity and reliability of outcome measurements in your clinical trials and help sites participate in studies without delays. Study Start-up We offer fresh solutions backed by deep data resources to accelerate and refine investigator and patient recruitment and site identification, so you can reduce trial costs and timelines while enhancing enrollment and quality. An i3 project management team tailored to your study’s unique needs, including such factors as therapeutic experience and location, can meet your most demanding requirements for quality, responsiveness, speed, and economy. Investigator Meeting Planning Coordinating the communication and workflow of busy professionals across the globe requires logistical expertise and complete familiarity with your study. i3 will manage this for you, taking meeting planning off of your hands so you can concentrate on the next task. Whether face-to-face or virtually, short term or long term, i3 will ensure seamless interaction and expert training that will set the stage for study success. Study Feasibility i3 provides accurate feasibility by embarking on a detailed six-step process that includes historical metrics from actual trials. This process is critical to understanding the history, challenges and relevant marketplace for your trial and can assist you in planning for success. Our resources include people and data tools to help you make smart decisions throughout each phase of your trial. Our comprehensive regulatory affairs expertise enables us to serve as your one-stop regulatory solution, ready to meet or exceed your regulatory goals for any project, at any phase, virtually anywhere in the world.
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