Register™

regulatory affairs tracking system

Aris Global believes that when it comes to regulatory affairs, compliance is not simply a document, it's a process that ensures that data is complete, accurate, approved and available to stakeholders and regulatory authorities across each product's entire lifecycle.

Automating regulatory submission tracking

Used by four of the top ten pharmaceutical companies, Register™ is the market-leading solution for centrally managing products and tracking global registrations across each product's entire lifecycle. Using Register, organizations have a single, integrated regulatory submission software solution for establishing full control of all regulatory affairs activity on a global basis.

Register captures and stores detailed product information and allows authorized users to track and monitor the drug/device product, country and company specific registration data at the global and/or at the local level.

Mitigates risk by providing a global view of the enterprise

Register provides a planning module that enables organizations to manage the numerous activities and resources associated with global regulatory submissions.

Eliminating the need for time-consuming manual processes, Register automates the definition, distribution and reporting of project plans at the global and local/regional level. As a result, Register improves visibility across the organization, giving users and management a global view of potential delays and resource conflicts, and enabling faster, informed decision making at lower cost.