From designing your CRFs, to ensuring the data delivered at the end of the trial is of the highest quality, we provide full-service data management functionality for your project. But, as a specialty service provider, we can customize our services to meet your specific project requirements including budget and timeline. Need support for a specific function, e.g. database build or data entry? We can help. Just need some expert advice on CRF design? We can help there also. Looking for a CDM team to get started quickly and manage the whole process? We typically get studies started in days, not weeks.
Considering we view the Clinical Data Management function as the “hub” of the clinical trial activity, we take the process seriously and we feel specific experience can be useful to your specific project. This helps ensure potential risks are identified and mitigated early in the process. Beyond our strong therapeutic experience, our data management teams have specific experience in the following areas:
- Phase I-III studies
- Phase IV studies
- Registry studies
- Medical device studies including pilot, feasibility, clinical evaluation, observational, and home-use studies
- Electronic Data Capture (EDC) studies
- Marketing surveys
Combining our experience and industry knowledge with our proprietary ClinPlus® DM and EDC system, our solutions can be entirely customized to fit your project scope and budget –pivotal Phase III submission studies, or small clinical evaluations, our CDM teams can serve as your “data communication center” for the entire project.