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Enhancing Commercial Strategy with Veeva Compass National

Overview of Veeva Compass National

Veeva Compass National is a cutting-edge solution that provides projected prescriptions and procedures data at the state and national level for both retail and non-retail products, covering over 4,000 brands in the U.S. market. This innovative product is designed to support commercial operations such as forecasting, market share tracking, and developing effective commercial strategies. It offers a more comprehensive and transparent view of the market, considering the evolving distribution channels in the pharmaceutical industry.

Key Features and Impact

With access to Compass National, users benefit from high-quality, transparent projected data encompassing over 4,000 brands, a 3-year history, and more than 5.9 billion annual total transactions. This comprehensive data enables organizations to understand pharmaceutical brand performance, gain insight into total prescriptions and procedures, projected total and new patients, and drive efficient commercial strategies. Users can leverage the unlimited data access to inform performance reporting, forecasting, and market share, ultimately making data-driven decisions with confidence.

Customer Testimonial and Feedback

According to Mike Rifflard, Vice President of Operations at ANI Pharmaceuticals, the implementation of Veeva Compass has significantly accelerated their product launch initiatives by providing field teams with a complete and timely view of their customers. This testimonial underscores the practical impact and effectiveness of Compass National in real-world commercial scenarios.

Resources and Further Exploration

For those seeking more information or interested in exploring the capabilities of Veeva Compass National, various resources are available, including blog posts, articles, videos, and product briefs. These resources delve into topics such as leveraging modern prescription and procedure data for commercialization, finding new prescribers for improved territory alignments, and driving patient-centricity through modern data analytics.

Enhancing Regulatory Compliance with Veeva Quality Vault Registrations

Overview of Vault Registrations Solution

Veeva Quality Vault Registrations is a powerful tool that assists organizations in tracking global product registrations and associated changes efficiently. This solution enables sponsors to plan, track, and report on product registrations worldwide, including health authority correspondence and commitments. With Veeva Quality Vault Registrations, users can manage product changes comprehensively, from initial assessment to submission creation, health authority interactions, and final registration updates. Moreover, the software allows for the monitoring and management of label changes at both the global and local levels. Registrations generated by this platform are compliant with regulatory standards such as xEVMPD and IDMP, essential for meeting EU regulations. Additionally, the inclusion of dashboards and reports provides insight into the progress of change events and aids in understanding product registration status across various regions.

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Revolutionizing Clinical Trials with Veeva Vault EDC

Efficiency and Agility in Clinical Data Management

Veeva Vault EDC, part of the Veeva Vault Platform, offers a cutting-edge solution for the challenges faced by today's complex clinical trials. This Electronic Data Capture (EDC) system provides a comprehensive environment for the collection, review, and processing of critical trial data related to patient outcomes. One of the standout features of Vault EDC is its ability to streamline the study initiation process. Users can effortlessly design patient forms and incorporate edit checks without requiring custom programming, saving valuable time and resources. This ease of use extends into the study execution phase, where Vault EDC efficiently collects patient form data, local lab results, medical coding, and implements quality controls such as querying, source data verification, and handling protocol deviations. Importantly, the database remains operational even during protocol amendments, ensuring uninterrupted study progress.

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