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Revolutionize Your Regulatory Processes with Veeva Vault Registrations

Enhance Regulatory Compliance with Veeva Vault Registrations

Veeva Vault Registrations is a cutting-edge solution designed to help pharmaceutical companies keep pace with evolving regulations. This platform enables sponsors to efficiently plan, track, and report on global product registrations while managing health authority correspondence and commitments. By leveraging Veeva's flexible data model, users can easily adhere to the latest IDMP standards and ensure regulatory compliance.

Streamlined Registration Management and Improved Data Quality

Vault Registrations streamlines registration management by reducing data duplicates and discrepancies, thereby improving overall data quality. Through this platform, companies can gain global visibility into the marketing status of their product portfolio, enabling informed decisions and enhancing regulatory oversight. With the ability to manage product registration queries and commitments efficiently, users can expedite health authority responses and stay ahead of critical deadlines.

The Impact of Vault Registrations on Regulatory Processes

Veeva Vault Registrations has significantly impacted the regulatory landscape, with the top 20 companies utilizing Vault RIM to streamline their processes. By consolidating 88 IT systems into one platform, companies have experienced a 90% reduction in written standards. This demonstrates how Vault Registrations can help companies exceed expected outcomes and enhance operational efficiency in regulatory tasks.

Customer Success Stories and Testimonials

Vault RIM has garnered trust from over 400 top and emerging biopharmaceutical companies, with users praising the platform's ability to accelerate decision-making processes. Joe McLaughlin, Head of Regulatory Business Practice and Innovation at Sanofi, highlighted how decisions that once took days or weeks can now be made within minutes, showcasing the transformative impact of Veeva Vault Registrations on regulatory operations.

Resources and Support for Regulatory Excellence

Veeva offers a range of resources and support tools to help companies optimize their regulatory processes. From the IDMP readiness center to industry insights and customer success stories, Veeva equips users with the knowledge and tools needed to navigate the complex regulatory landscape effectively. By joining the conversation in Veeva Connect, customers can interact with product leaders and peers to share insights and best practices.


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Revolutionizing Clinical Data Collection with Veeva Vault EDC

Introduction to Veeva Vault EDC

Veeva Vault EDC is a cutting-edge Electronic Data Capture (EDC) solution that revolutionizes the process of collecting, reviewing, and processing trial data pertaining to patients. With a focus on handling the complexities of modern clinical trials, Veeva Vault EDC offers an end-to-end environment that streamlines the entire data capture process.

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Empowering Commercial Execution with Veeva Commercial Cloud

Overview of Veeva Commercial Cloud

Veeva Commercial Cloud serves as the technological backbone for commercial execution, facilitating seamless collaboration between sales, service, marketing, and medical teams. By leveraging the integrated capabilities of Veeva Data Cloud, this platform offers a comprehensive suite of interconnected software and data solutions that drive enhanced insights, innovation, and operational efficiency.

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Enhancing Collaboration with Veeva Vault's Collaborative Authoring Solutions

Unleash the Power of Collaboration

Veeva Vault's Collaborative Authoring solution, integrated with Microsoft Office™, revolutionizes the way users can work together on document creation and editing. With the ability for multiple Vault users to simultaneously collaborate on Office documents using Office desktop software, Office Online™, or Office mobile apps, teams can boost productivity, streamline workflows, and enhance communication in real-time. This innovative feature enables seamless collaboration across different locations and time zones, fostering a more dynamic and efficient work environment.

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Revolutionizing Submission Publishing with Veeva Vault Submissions Publishing

Simplified Submission Generation

Veeva Vault Submissions Publishing is a comprehensive solution that streamlines the generation of electronic submissions for global health authorities. By continuously updating templates and validation criteria to align with evolving regulations, Veeva ensures that users can always stay compliant and submit accurate documents. This proactive approach significantly reduces rework and delays in the submission process, ultimately improving efficiency and saving valuable time.

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