Welcome to Knowledge Base!

KB at your finger tips

This is one stop global knowledge base where you can learn about all the products, solutions and support features.

Categories
All

Products-Veeva MedTech

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.

Comprehensive Repository of Submission Published Output

Vault Submissions Archive serves as a global and secure repository that houses all submission published output. It acts as the definitive source of applications that have been submitted to health authorities, offering organizations a robust platform for managing critical documentation. Users can leverage the viewer, which supports a wide range of electronic and paper formats, with convenient PDF link navigation for electronic submissions.

Enhanced Visibility and Accessibility

One of the key features of Vault Submissions Archive is its ability to provide enhanced visibility and accessibility to regulatory documents. Users can effortlessly view submissions, health authority correspondence, and all previously submitted applications in one centralized location. The embedded document viewer offers a detailed look into the structure of each document, facilitating easy navigation and understanding.

Empowering Global Regulatory Readiness

Vault Submissions Archive empowers organizations to maintain global regulatory readiness by allowing remote team members to access authorized submissions from anywhere in the world. This capability ensures that teams can collaborate effectively and stay compliant with regulatory requirements, even in a distributed work environment. By consolidating submissions from regional offices and local affiliates, organizations can ensure a cohesive approach to regulatory compliance.

Optimizing Efficiency and Performance

With Vault Submissions Archive, organizations can optimize efficiency and performance in regulatory compliance management. Dynamic search, filtering, and navigation tools enhance user experience, making it easy to find and retrieve relevant information. By simplifying submission tasks, saving time on approval processes, and consolidating legacy systems, organizations can achieve impressive results, with 80% of submission tasks eliminated or simplified, over 200 hours saved on approval and renewal reporting, and 65 legacy systems consolidated.


Stay Ahead in Today’s Competitive Market!
Unlock your company’s full potential with a Virtual Delivery Center (VDC). Gain specialized expertise, drive seamless operations, and scale effortlessly for long-term success.

Book A Meeting To Setup A VDCovertime

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.

Read article

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.

Read article

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.

Read article

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.

Read article

Streamline Regulatory Submissions with Veeva Vault Submissions

Efficient Regulatory Document Management

Veeva Vault Submissions is a robust content management platform that streamlines regulatory submissions by providing a comprehensive solution for planning, authoring, reviewing, and approving regulatory documents. With its enterprise capabilities, Vault Submissions simplifies the process of creation, version control, approval, and real-time co-authoring of all submission-related documents. This ensures that regulatory teams have a centralized platform to collaborate and manage their submission documents efficiently.

Read article