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Five offices strategically located in England and Scotland create a strong base for us to provide complete clinical monitoring capabilities via experienced field-based monitors, full-service regulatory consulting and data management capabilities.
Our European Headquarters is in Crowthorne and serves as a focal point for providing comprehensive Phase II–IV clinical services such as protocol design, feasibility and site selection, regulatory document collection, monitoring and site management, project management, resourcing, clinical quality assurance, clinical data management, statistics, medical writing, information technologies, post marketing surveillance and health economic/outcomes research services.
Our offices in Scotland provide access to a region that is home to cutting-edge areas, such as biomanufacturing, bioinformatics and stem cell sciences. In addition, there is more medical research conducted per capita in Scotland than anywhere else in Europe.
While the majority of our work is in Phases II–III, an increasing proportion is in post-marketing surveillance. We now provide full services for clinical trials in the United Kingdom plus contract site coordinators.
We also provide professional training on various topics related to clinical research as part of our corporate training and development division, Kendle College.
In addition, we provide regulatory consultancy and support from our office in Ely, Cambridge. See the EU Regulatory section below for more information. |
