Presented By:

Paul Marini, Quality & Regulatory Systems Leader / Quality & Regulatory Operations, Becton Dickinson

Sameer Kadam, Senior Solutions Consultant, Sparta Systems, Inc.

You know the importance of product registration relative to meeting financial objectives. Time to market is critical. In a recent survey of Top 50 Medical Device Companies, we found that 7 out of 10 companies manage the product registration process in paper or through complex Excel spreadsheets that are labor intensive and lack real time visibility and control. Companies can vastly improve productivity and reduce the risk of errors or re-work by adopting software to enable the global product registration process.

In this webinar, you will hear a case study that illustrates how global registration tracking can be made more efficient and less risky using new tools. Join us to learn how your team can:

• Provide real-time access to a firm's registration and submission status as well as to all related work items, commitments, and tasks
• Improve cycle time of approvals by ensuring accurate data and streamlined management of all registration data and submission activities
• Increase responsiveness and accuracy of registration data for all devices, products, indications, formulations and health authorities
• Safeguard against costly errors that can occur when accurate registration information is not readily available
• Enhance overall collaboration between Regulatory Affairs and supporting departments

Who Should Attend

Regulatory and quality product managers who are involved with the product registration tracking process.