Whether your project is standard or complex, our Early Phase Business Unit (Phase I/IIa) has a dedicated, streamlined approach that helps ensure we complete your study on schedule and on budget. Our goal is to exceed your expectations. Each and every time.
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As a mid-sized CRO, we consider ourselves to be the “right size” outsourcing partner. While we are small enough to provide you with a personal touch and keep the focus where it belongs—on you, with a global reach across 32 countries, in all the key drug development markets, we are also big enough to conduct large and complex global trials and support your larger IIB and III studies.
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Your drug received approval and is now on the market. But that doesn't mean the clinical development process is over. In fact, Late Phase (Phase IIIb/IV) trials are more important than ever. Whether it's a proactive investigation into health outcomes, a safety surveillance study, Risk Evaluation and Mitigation Strategies (REMS), or leveraging a competitive advantage with a label extension, Late Phase research is a valuable commercial investment. Our team of experts helps you create a customized Late Phase study designed to achieve your particular goals and objectives — while also staying on-time and on-budget.
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Whether you're investigating an apparatus, instrument, machine or other type of device, our Medical Device Business Unit knows your success hinges upon highly specialized regulatory, reimbursement programs, safety and marketing support. Operating on high-quality systems, we can prepare those key documents that will ultimately clear your product for marketplace entry.
Even after your commercial launch, we're here to help propel your device to that next level. From developing a reimbursement strategy to meeting post-marketing surveillance requirements, we offer the added value of a long-term relationship that endures throughout every phase of your device's lifecycle.
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Our experienced technical team services your project at a local geographic level with a large, global enterprise solution supporting these key services: Clinical Data Management, Biometrics, Medical Writing and eTechnologies. Our goal is to provide an outstanding customer experience, with high-level expertise and cost competitive packaging. At the same time, we strive to be the premier CRO in the acquisition, analysis, interpretation and presentation of our clinical data solutions. Whether you partner with us for an FSP engagement, standalone work or a full-service project, we use the same quality processes. Our holistic approach is just one of the reasons why we have so many repeat customers.
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For over 17 years, our people have been designing and implementing packaging to simplify even the most complicated dosage regimens. And with our global presence, we provide cost-effective, timely delivery of your study medications and medical devices anywhere around the globe. In fact, our office is located just minutes from a major international airport hub.
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