Our Technology - tried and tested on over 400 studies

After four man-years of development, the newest version of our data management system, Syneclin II, has been commissioned. Fully validated to the highest specifications and 21 CFR Part 11 compliant, it has been designed to incorporate CDISC (Clinical Data Interchange Standards Consortium) standards, which are our defaults.

Our Internet-based module is perfect for remote data entry and management. Entry screens just like the CRF are created from existing validated CRF modules. Data entered at the clinical trial site is collected via the Internet using a secure encrypted environment.

Whether EDC or paper based, data can be made available for rapid review, providing your clinical team with data in the format they want and when they want it. This functionality has been highly acclaimed by many clinical professionals.

In addition, Syneclin.net allows data to flow between on-line systems and Syneclin II. It can enter data directly into our Sponsor’s database on their servers, allowing them to hold their own data locally if desired.

Syneclin II provides an easy interface for data browsing and reporting on demand. Reports are created in a clear, easy-to-read format. In addition, integrated software removes the potential bottleneck of database development, allowing the database to be ready when the first patient is enrolled.

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