TrackWise can help regulatory affairs organizations devote more time to activities that directly contribute to the product approval process and increase their value to the organization. TrackWise improves the management of product life cycle activities for each registration, in each country, and for every dose, indication and formulation or device classification and 510k number.

This session, will teach you how TrackWise can be used to manage the workflow and critical data associated with product registration tracking and see a demonstration that shows TrackWise configured to support product registration tracking. During the hour you will learn how TrackWise:

• Streamlines regulatory affairs workflow and improves time to market by providing users with efficient tools to replace manual tracking processes
• Guarantees real-time access to registration and submission status as well as to all related work items, commitments, and tasks
• Improves cycle time of approvals by ensuring accurate data and streamlined management of all registration data and submission activities
• Increases responsiveness and accuracy of registration data for all devices, products, indications, formulations and health authorities
• Enhances overall collaboration between regulatory affairs and supporting departments