SYQUENCE is guaranteed to simplify your global registration and transparency
compliance efforts. Our web-based system is designed to streamline your process and reduce the work of your resources by standardizing your data. Standardized data is shared across a series of structured forms to produce consistent disclosures into the public domain.
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Sylogent, with more than ten years of experience with protocol registration and results disclosure, has designed a system that dramatically simplifies these processes by automating much of the work. The system automatically shares the data from an approved Master Form, saving hours of manual data entry. SYQUENCE can publish approved records to clinicaltrials.gov and a client-branded registry and will generate an approved XML file for EudraCT upload.
Since its founding, Sylogent has been focused on, and even become synonymous with, simplicity. Simplicity drives our development teams to design tools that are intuitive for all users and that add value by making processes and resource efforts easier. The system is available anytime and system users just need internet access and a modern browser (Internet Explorer, FireFox, Chrome or Safari).
With our automated development process, SYQUENCE can be deployed and ready to use within days. The system includes an integrated training module that assists with user on-boarding. The migration utility instantly downloads sponsor records from clinicaltrials.gov and EudraCT. The unique system configuration enables users to modify records quickly and get them approved for publishing.
One of the best features of SYQUENCE is the affordable pricing options for any size company. SYQUENCE is designed to deliver the best ROI when compared with all company systems, year after year. Clinical Trial Registration & Results Disclosure is a required task for all study sponsors, and SYQUENCE guarantees to help make it simple, easy and fast while saving you significant costs.