Every clinical trial is a scientific experiment and the clinical data generated is the key output of this experiment. All the people and processes involved in a trial tirelessly work with one goal in mind: to obtain complete, accurate and timely data for objective decision-making by drug developers, medical staff, investors and regulators. In other words, clinical trial data should be valued like gold dust, not coal dust.
Since our beginning as a specialist data provider 20 years ago, Cmed has enjoyed a reputation for providing expert data services. We now boast a team of 140 strategically located staff for data and analytics, ready to help sponsors make fast and accurate deliveries, despite the increasing volumes, types and sources of data in clinical trials today.
Our clinical data scientists have demonstrated their skills in technical innovation and project delivery on over 700 studies ranging from rapid first in human studies, through trials with complex and adaptive protocols to huge registry studies involving over 10,000 patients.