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Empowering MedTech Organizations with Veeva Vault MedComms

Revolutionizing Medical Content Management

Veeva Vault MedComms is a cutting-edge solution designed to meet the unique needs of medtech organizations in managing their scientific content efficiently. Launched in 2012, this platform has garnered over 100 satisfied customers and is considered a highly mature product in the industry. MedComms offers a comprehensive range of features that streamline the entire lifecycle of medical content, from creation and review to approval, storage, and distribution.

Tailored Solutions for Medical Affairs

One of the key strengths of Veeva Vault MedComms is its ability to support the specific requirements of Medical Affairs departments within medtech companies. The platform allows for the smooth review and approval of content, along with the management of unique content types and workflows. MedComms also includes the Medical Portal, a centralized repository that facilitates controlled content distribution to various user groups, such as Medical Science Liaisons (MSLs). This feature enhances content reuse and ensures regulatory compliance.

Enhanced Connectivity and Integration

Veeva Vault MedComms offers seamless integration with other Veeva products, such as Vault CRM for MedTech and MedInquiry. This connectivity enables automatic distribution of approved scientific content and real-time responses to medical inquiries. The platform also provides an API for integration with third-party systems, allowing for a more cohesive and efficient workflow. By leveraging these integrated features, medtech organizations can maximize operational efficiency and maintain consistency in their content delivery.

Driving Efficiency and Consistency

With Veeva Vault MedComms, medtech organizations can centralize their medical content management and scale their operations effectively. By ensuring real-time access to up-to-date approved content, teams can respond rapidly to medical inquiries and maintain consistency across different communication channels and geographical regions. The platform also offers insights into content usage patterns, helping organizations track user activity, channel preferences, and interactions to optimize their content strategies.

Empowering Learning and Innovation

Veeva provides a range of resources to help medtech organizations leverage the full potential of Vault MedComms. From innovation guides to white papers and blogs, users can explore best practices for digitizing scientific communications, maximizing Key Opinion Leader (KOL) impact at medical congresses, and more. By continuously learning and innovating with Veeva Vault MedComms, organizations can stay ahead of the curve in the dynamic medtech landscape.

Optimizing Medtech Solutions with Veeva MedTech Professional Services

Efficient Deployment for Medtech Solutions

Veeva MedTech's Professional Services team is dedicated to ensuring the efficient deployment of medtech solutions for companies of all sizes, from small startups to global industry leaders. With a structured and iterative approach, Veeva guides clients from project initiation to successful implementation, reducing the burden on internal teams and delivering solutions on time and within budget. This streamlined process prepares users for seamless adoption and equips companies with compliant, high-quality products that reach patients swiftly.

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Unlocking the Benefits of Modern Claims Management with Zeiss and Veeva Vault PromoMats

Zeiss Embracing a Modern Approach to Claims Management

Jochen Tham, the Head of Digital Marketing at Carl Zeiss Meditec, highlights the advantages of adopting a modern and systematic approach to claims management. By leveraging Veeva Vault PromoMats, Zeiss is able to streamline and optimize their claims process, leading to improved efficiency and effectiveness in how they manage their promotional materials.

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Empowering Global Regulatory Compliance with Veeva MedTech's Advanced RIM Solution

Streamline Global Regulatory Compliance and Information Management

In today's rapidly evolving landscape of globalization, intricate supply chains, heightened focus on patient safety, and constantly evolving regulatory frameworks, achieving and maintaining global regulatory compliance has become a complex challenge for medical device and diagnostics manufacturers. Traditionally, managing compliance involved juggling numerous systems and spreadsheets, leading to manual, inefficient processes and delayed time to market. However, Veeva MedTech's Vault RIM Platform offers a transformative solution by providing a centralized hub for registrations management, submissions, publishing, and archival processes. By offering a single source of truth, this platform empowers organizations to streamline their regulatory compliance efforts and expedite time-to-market for their products.

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Unlocking Efficiency and Agility in Clinical Trials with Veeva Vault EDC

Streamlined Data Capture Process

Veeva Vault Electronic Data Capture (EDC) revolutionizes the way clinical trials handle data collection, review, and processing. With over 100 satisfied customers worldwide, Vault EDC offers a comprehensive platform to manage patient information throughout the study lifecycle.

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Veeva MedTech Vault Quality Platform: Streamlining Quality Management for MedTech Companies

Transforming Quality Management

In today's fast-paced medical technology industry, ensuring the highest quality and regulatory compliance is paramount. Veeva MedTech's Vault Quality Platform offers a comprehensive solution to streamline quality management for medical device, diagnostic, and therapeutic companies. By unifying global processes, content, and functions on a cloud-based platform, organizations can achieve audit readiness, ensure compliance, and accelerate innovation.

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