A Complete Suite of Superior Solutions, Clinical Data Management, Biometrics and Medical Writing—all Wrapped with eTechnologies.
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.
Consider the advantages:
Functional Service Provider (FSP) Relationships. More of our customers are trending towards these long-term strategic engagements and our model focuses on efficient resources management and quick scale-up. We understand that a lot can change in your study portfolio, so our model prepares for any situation. We have a core set of resources dedicated to your organization, but also offer flex resources—such as additional professionals who are cross-trained on your work and empowered to step in and perform work during peaks. It’s an infrastructure that helps keep costs low and productivity high.
CDISC Leadership. Since our first CDISC submission in early 2004, we’ve upheld a commitment to helping clients implement these standards. In fact, we were one of the first CROs to submit a CDISC application and our Biometrics team is a CDISC Registered Solutions Provider.
Robust eTechnology Portfolio. Our traditional paper system is powered through Oracle® Clinical, the industry standard. We also offer a robust in-house EDC system portfolio that can be leveraged to fit your particular study, whether it’s simple or complex and global, while multiple technology transfers also allow our people to perform the work. We've performed 150+ EDC studies in the last 10 years in all phases and regions across many therapeutic areas.
Global Resources. Our worldwide team of professionals is located in the European Union, Asia Pacific region, the United States and Canada. Furthermore, our ever-growing data centers are strategically located around the globe in Australia, Germany, India, the United Kingdom and the United States. Centralized systems and communication maintain a constant flow of information.
Streamlined Database Build. Our INTREPID EDC process creates CDM and Monitoring role shifts, ensuring real-time review and freezing. In addition, our unique KickStart® Team manages your entire study database planning and build process. This group of experts works closely with you, external vendors and your Theorem Clinical Research Data Manager to define data requirements, design the eCRF, create the edit specifications, and manage the database build timelines to ensure a quality database is created on time, every time.