Whether you need expert advice on pivotal Phase III submission studies or a data management team for the entire program, our solutions can be custom-fit to the scope, budget and timeline.
From providing specific function support, to ensuring delivery of the highest quality data at the end of the trial, Medfiles Global provides flexible data management support for your project.
Because clinical data management is the core of all trial activity, you need the best eClinical technology, expertise, and processes to get the most out of your clinical data.
Our teams and vendors have specific data management experience in the following areas:
- Phase I-IV studies
- Registry studies
- Medical device studies including pilot, feasibility, clinical evaluation, observational and home-use studies
- Electronic data capture studies
For more information please contact
Clinical Research Services
+358 20 744 1504 / firstname.lastname@example.org