Ever wonder what fuels the success of a clinical trial? It boils down to collaboration—bringing together diverse teams of sponsors and Contract Research Organizations (CROs), often spanning multiple geographies. Sponsors take the lead by setting the course, securing funding, and ensuring that every regulatory requirement is met. They are responsible for designing the trial protocol, selecting sites, and making critical decisions to keep the trial on track.
For starters, much of the technology needed for personalized medicine is still nascent compared to other areas of healthcare delivery. The big data analytics required to reliably interpret patient DNA or genomics data is not yet readily available at all sites conducting research. In addition, sites that have access to this type of technology require highly specialized personnel – including genetic counselors, bioinformaticians, and biostatisticians– who are in high demand across many industries.
The Cloud Concinnity platform was built to meet the specific needs of clinical trial managers, CROs, and DSMBs. Our cloud-based system provides trial stakeholders with a centralized platform for patient information, communications, processes, and reporting onto a single, secure hub to improve their quality of life.
Improving data protection begins with creating a comprehensive data protection policy.
The policy can be as detailed or straightforward as your organization deems necessary. It should include:
Cloud Concinnity was specifically built to meet the need for more efficient, effective clinical trial management. Our cloud-based integrated platform centralizes, simplifies, and automates control of data, communications, process management & reporting while unlocking the value of big data.
Cloud Concinnity® is an integrated platform that centralizes, simplifies and automates control of data, communications, process management & reporting, while unlocking the value of big data.
