Clinical Applications

Synteract’s technology platforms allow for superior customization for each project, which provides sponsors with the most advantageous outcome. Our full-service infrastructure is very robust and has terrific scalability to meet your needs.

Project Tracking and Management Updated Daily

With Tenrox and our in-house CTMS data warehouse, we’re able to cogently track, manage, and report on projects in real time. The systems are updated daily, allowing sponsors to receive updated project status data in a timely fashion, while fortifying the corporate knowledgebase at Synteract.

Flexible Data Management Approaches

We have deployed a flexible set of database management systems to provide sponsors with myriad ways to approach data collection and management during a trial. We can automate patient enrollment at study sites with the set up of voice and/or web randomizations via our IVRS/IWRS platform. This can also be done for patient diaries as well. For study data, we can use the Clintrial system for paper-based trials, but can also opt for fax-only with DataFax or web/fax/paper simultaneously with SynCapture, our proprietary software that allows for sites to select a particular data collection method for a study. These options increase timely data acquisition and compliance.

Electronic Medical and Safety Report Assurance

Oracle AERS (along with our in-house SynCoder tool for medical coding) allows us to track, monitor, report, and submit safety data to regulatory agencies around the world. Electronic submissions can be performed via our E2B gateway set-up with Axway’s Synchrony product, giving us the ability to submit safety reports to EMEA (Europe) and FDA (US). Additionally, with AERS, we can set up clinical studies for safety tracking, or even host the product for sponsors, saving you the costs of implementation, validation, resources, and support.

Fast Turnaround on Biostatistics and Data Reporting

Complete with an experienced and savvy staff of biostatisticians, we can provide solid and dependable analysis on study data using the SAS System. This de facto programming standard within the industry allows us to give sponsors the results from study findings. Other tools, such as Integrated Review and our secure web portal (customized for every sponsor,) provide for access to published applications and ad-hoc reporting on study data in real-time.