Veeva Registrations

Overview

The platform facilitates the planning, tracking, and reporting of global product registrations while managing correspondence and commitments with health authorities. It is designed to handle product changes from assessment through to the creation of submissions, interactions with health authorities, and updating final registrations. The system enables tracking and management of label changes at both global and local levels. Additionally, it generates compliant product data outputs such as xEVMPD and IDMP for EU regulations.

Dashboards and reporting tools offer insights into the progress of change events and help comprehend product registration across different locales.

Benefits

• Improve Data Quality: Streamlines registration management by reducing data duplicates and discrepancies.
• Global Visibility: Provides a complete view of the marketing status of the global product portfolio.
• Efficient Responses: Manages queries and commitments related to product registrations to meet response deadlines promptly.

Impact

Adoption statistics indicate that 15 of the top 20 companies utilize the system, achieving a 90% reduction in written standards and consolidating 88 IT systems into one unified platform.

Customer Insights

Users appreciate the detailed insight it provides into submissions, considerably reducing the time taken for decision-making and facilitating global change management.