At Continental Clinical, we know the importance of Investigators and Sites who understand the collection and presentation of patient and investigational product data is as valuable as its content.
We have focussed on upgrading user experience, with improved telecommunications, consumer experience, data tracking and data exportation.
Partnerships have allowed us to fully integrate paperless data collection into this paper-intense reality of clinical research.
EMR or old school handwritten charts, we manage translate and transmit data in clean formats to our stakeholders.
"The goal is to turn data into information, and information into insight – Carly Fiorina, chief executive at Hewlett-Packard
At Continental Clinical, we know the process of obtaining regulatory approval can pose numerous obstacles, from elongated timelines, to IRB corrections and Protocol revisions. We have specialists that can navigate through the most complicated regulatory landscapes.
From legal counsel, to daily administrative upkeep, we focus on details so you can focus on the discipline of the study itself
Continuity is key in trials and we understand the importance of having Clinical Research Coordinators (CRCs) that see a study through from start to finish.
We have certified staff that is cross trained across all of our studies. Quality suffers because knowledge transfer between CRCs is never perfect. Therefore, our cross training equals a transparency that affords each person in our staff a 360 degree understanding of their study.