​Rationale for this service:

• All clinical trials utilize an EDC system, which is a great software to capture clinical data at site, however, EDC systems are NOT designed to review data.

• Many sponsor companies do not have a dedicated tool to review the data, on a real-time basis. 

• Without having any data oversight tool, it’s not uncommon for many critical data to be missed, or entered inconsistently, which could adversely affect the conclusion of the trial.

• And therefore, consistent oversight of the clinical trial data is critical for the success of the trial.

Our approach:

• We begin with aggregating all study data in one place, and organize the data in a clean, readable format.

• Once all data is in one place, we constantly refresh it to keep it updated real-time. 

• Now, we can run custom checks on the data to identify any issues, create patient profiles for manual data review, monitor desired lab values for patients, and view all important study reports on a 'Project Dashboard'.

• Combined everything, the study team will have full visibility and control of their study data.