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It’s a promised standard underlying our full suite of CRO services that includes expertise, mentoring, custom planning, and collaborative support from a team of experts who understand your needs.
Our goal is always to help you succeed by working as a partner to your team. As your contract research organization, we will tailor a project plan to meet the needs of every project. Whether you need full scope global services or only one particular service offering like Data Management or IVRS, our team of experts is here to help.
ICD+ (Intelligent Clinical Development) is the approach we use to take time and cost out of the drug development process. Let’s face it, the cost of bringing a new therapy to market today is 600% higher than it was in 1979, according to the Office of Health Economics, “CMRI: Data Report, 2011”. The Tufts Center for the Study of Drug Development in Boston goes even further in 2013, stating that annual revenue of $1 billion is needed to recoup research, development and marketing costs. Those numbers are just not sustainable!
SynteractHCR has developed our ICD+ platform to leverage our deep clinical development expertise, appropriate technology, and optimized process execution to drive solution-oriented efficiencies and consistent standards on a global scale. Our therapeutic and clinical development history shows we have the experience to guide you, taking you through the trial continuum from early planning to post-marketing, and to offer alternative solutions when needed. We have the methods and client advocacy program to support compliance. Plus our Clinical Intelligence Portal offers transparency – user-friendly access to data via an online dashboard that allows you to see project status in a timely and efficient manner.
Trust us to innovate with you to define the most efficient approach and proactive assessment to achieve your goals and streamline your trials.