The ICMJE, FDA, EMA and other international regulators are aggressively pushing for more public disclosure of protocol and trial related information. These regulations not only compress timelines for resource limited organizations but also requires that the data being shared is delivered on time and is consistent with all data shared by the organization.
You need more than a publication database.
Sylogent offers an integrated set of tools to help ensure you satisfy regulatory milestones and maximize data sharing across critical documents. From structure protocols, compliance planning and data disclosure to target selection, author documentation and publication approvals, our software and services can help.
PUBSTRAT is a robust, highly configurable tool that streamlines your entire publication development and execution process. PUBSTRAT organizes your information and facilitates collaboration between all stakeholders, while providing full transparency into your publication planning process. The system manages the manuscript review and approval process from planning through final submission. Teams can track all the details from a single view.
PUBSTRAT includes access to Journal Selector and Conference Authority, so you can easily identify the right journals and conferences to reach your target audiences. Abstract deadline and meeting dates are updated regularly, so that you publish on time and with minimal effort. CITE CENTRAL stores and manages all citations and documents.
Program Budgeting & Planning
Study Data Management
Project Workflows & Management
Automated Spend Tracking
Task Notifications & Alerts
Author Documentation Compliance
Reports & Dashboards
We understand the overall issues across your company.
We work with all of the business units today.
We can help you transform your company - with minimal disruption.