Getting the Right Information for Your Trials
Our clinical research multi-disciplinary team - biostatisticians, operations experts, programmers, data managers, and medical writers - draws on their extensive knowledge and clinical experience to help you meet the challenges of designing and implementing complex trials head-on.
[fa icon="check"] Support for DMCs
[fa icon="check"] Randomization Services
[fa icon="check"] Clinical Data Management
[fa icon="check"] Biostatistics
[fa icon="check"] Statistical Programming
[fa icon="check"] Medical Writing
[fa icon="check"] CDISC Migration
[fa icon="check"] Regulatory Submissions
[fa icon="check"] Functional Services
Our goal is to improve the Probability of Success of your development efforts. Long established leaders in the design and implementation of adaptive trials, we are also well regarded for our clinical data handling capabilities including end-to-end data management solutions.
Cytel adaptive designs, trial analytics and clinical data know-how have supported numerous successful programs resulting in approved products across a range of therapeutic areas including oncology, cardiovascular, gastric/intestinal, and rare, orphan diseases.
Cytel has helped numerous sponsors considerably improve product ENPVs by identifying and eliminating unnecessary trials, those contributing little useful information towards your trials likelihood of success.