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Optimizing Claims Management in MedTech: Insights from Phillips and Fresenius Medical Care

The Importance of Effective Claims Management

In the dynamic landscape of medtech, effective claims management plays a pivotal role in commercial success. Often overlooked, claims are instrumental in determining product pricing, market access, and overall competitiveness. Philips and Fresenius Medical Care recognized the need for a centralized claims library to mitigate compliance risks, streamline processes, and enhance marketing strategies.

Modernizing Claims Management Processes

Both companies acknowledged the necessity of modernizing their claims management processes. Daniel Milliken of Philips emphasized the critical role of claims in establishing product value and pricing strategies. Similarly, Fresenius Medical Care, led by Jessica Pavic, aimed to align its claims management system with industry standards and enhance product credibility through substantiated claims backed by robust clinical evidence.

Incentivizing Organizational Change for Enhanced Compliance

Organizational buy-in for claims management transformation can be challenging. Milliken and Pavic employed different approaches to drive change within their companies. While Milliken highlighted compliance risks to emphasize the need for a centralized claims library, Pavic focused on showcasing the additional benefits of efficiency and speed to engage marketing teams. Both approaches underscored the importance of aligning internal stakeholders towards a common goal of compliance and operational efficiency.

The Claim-to-Clinical Connection: A Strategic Imperative

Connecting claims management with clinical evidence early in the product development lifecycle emerged as a strategic imperative for both companies. By integrating cross-functional teams to align R&D, marketing, and clinical efforts, medtech companies can generate evidence, substantiate claims, and craft a cohesive value proposition. Pavic and Milliken emphasized the need for proactive claims management from the clinical trial stage, highlighting the significant time investment required to substantiate claims effectively.

Future Trends in Claims Management

While Philips and Fresenius Medical Care are at different stages of claims management optimization, both are exploring avenues for further enhancement. From automating processes to fostering system connectivity, the focus remains on improving efficiency and effectiveness in claims management. Pavic highlighted the benefits of a centralized claims library in enabling omnichannel content creation, while Milliken reiterated the importance of establishing efficient processes pre-launch to ensure product success.

Vault Submissions Archive: Revolutionizing Regulatory Compliance Management

Efficiently Managing Regulatory Dossier Lifecycle

Veeva Vault Submissions Archive is a cutting-edge solution designed to streamline the management of the regulatory dossier lifecycle. With this tool, organizations can access a comprehensive record of all regulatory submissions, creating a centralized repository for critical documentation. By maintaining a complete history of submissions, users can easily track the evolution of each application and ensure compliance with regulatory standards.

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Revolutionizing Clinical Data Management with Veeva MedTech's Vault CDMS

Introduction to Vault CDMS

Veeva MedTech's Vault Clinical Data Management Suite (Vault CDMS) is a cutting-edge software solution that aims to revolutionize the way medtech clinical teams manage trials. By unifying electronic data capture (EDC), auto-coding, and study data forms optimization, Vault CDMS provides complete control over trial configurations and management, empowering clinical teams with agility and speed.

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Optimizing Global Claims Review and Approval with Veeva Vault PromoMats

Streamlining Processes for Global Claims Management

In today's fast-paced healthcare industry, efficient management of global claims is crucial for companies like Fresenius Medical Care. Veeva Vault PromoMats offers a comprehensive solution to streamline the review and approval processes for claims worldwide. With this innovative platform, companies can expedite the review of claims, ensure compliance with regulations, and ultimately accelerate time-to-market for their products.

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Maximizing Quality Control with Veeva MedTech Vault Quality Platform

Empowering Global Quality Management

In today's fast-paced and highly regulated medical industry, ensuring the highest quality standards while accelerating product development is crucial. Veeva MedTech's Vault Quality Platform offers a comprehensive solution that enables companies to deliver superior products faster while maintaining compliance with regulatory requirements. By unifying quality management processes on a global scale, the platform facilitates seamless collaboration and provides real-time insights for trend analysis and rapid innovation.

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Optimizing Regulatory Compliance with Veeva Vault Submissions Publishing

Streamlining Submission Processes

Veeva Vault Submissions Publishing is a comprehensive solution designed to streamline the submission process for global health authorities. By generating electronic submissions, this tool eliminates bottlenecks and significantly accelerates the delivery of critical documentation. With continuous publishing capabilities, regulatory teams can stay ahead of evolving regulations by utilizing up-to-date templates and validation criteria provided by Veeva. This ensures that submissions are always compliant and delivered on time.

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