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As a full service CRO with two decades of experience directing Phase I – IV clinical development programs leading to more than 230 product approvals, SynteractHCR has proven it is uniquely positioned to help clients successfully navigate the complex drug development process.
We understand that intelligent clinical development, where time and cost are reduced, is critical to the long-term success of our biopharmaceutical clients.
Our Intelligent Clinical Development Approach Ensures Clear Focus
Our deep culture around service means we collaborate with every client to tailor an approach to fit your specific project needs, offering guidance across the spectrum of Phase I – IV clinical studies. Intelligent Clinical Development or ICD+ is the platform we use to leverage our deep clinical and therapeutic expertise, appropriate technology, and optimized process execution to drive solution-oriented efficiencies on a global scale. ICD+ allows sponsors to get to decision points faster, while providing high quality, a uniform approach, and consistent standards internationally.
We provide broad therapeutic expertise with depth in specialty segments, For example, we’ve become the go-to oncology CRO for many clients. As a qualified clinical development CRO, we focus together on your goals from the outset, and strategically adapt services for each project, to ensure every aspect of a project is planned for and delivered as promised at a competitive price.
We know that one size does not fit all when it comes to clinical development. Given nearly 90 percent of our business is referrals and repeat business, this clearly demonstrates SynteractHCR has been successful in its tailored approach, especially among emerging to mid-sized pharma, biotech, and device companies, a unique industry segment we have served since our founding.
At SynteractHCR, we foster enduring relationships with our clients and partners. We provide value through our actions – what we say is what we do. At SynteractHCR, responsive customer service isn’t just a phrase; it’s a promised standard that includes ongoing support from a specialized team dedicated to meeting or exceeding your expectations and accelerating your clinical development timelines.
Unsure if your study
is in need of a rescue?
SynteractHCR rescued 40+
studies since 2009
alone. We can help
you determine if
your entire study
needs a rescue
or just a part.