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Revolutionize Adverse Event Management with Veeva Vault Safety

Introduction to Veeva Vault Safety

Veeva Vault Safety, a cutting-edge individual case safety report (ICSR) management system, revolutionizes adverse event management for clinical and post-marketed products. This modern solution offers seamless support for the intake, processing, and submission of adverse events on a global scale.

Streamlined Global Adverse Event Processing

Within Veeva Vault Safety, sponsors and Contract Research Organizations (CROs) can efficiently process global and domestic adverse events related to drugs, biologics, vaccines, devices, and combination products. The system provides built-in gateway connections and reporting rules that streamline the management of case submissions to health authorities and distribution to partners.

Centralized Coding Dictionary Management

Veeva Vault Safety simplifies adverse event coding with automated management of coding dictionaries. This includes semi-annual updates for MedDRA, WHODrug, and EDQM, ensuring that sponsors and CROs maintain compliance with the latest standards and classifications.

Key Features and Benefits of Vault Safety

Vault Safety offers numerous advantages, such as streamlining adverse event management processes, automating intake through submissions, ensuring end-to-end safety processes, providing global case view and oversight, and facilitating compliance with new regulatory requirements through regular updates. Customers can leverage these features to enhance safety oversight, improve case processing efficiency, and stay ahead of evolving industry demands.

Customer Success Stories

Veeva Vault Safety has enabled organizations like Merck to streamline their processes and achieve unified safety oversight. Customer testimonials highlight the system's user-friendly nature, seamless integration, and intuitive design, emphasizing the transformational impact it has had on pharmacovigilance operations.

Resources and Further Learning

For those interested in learning more about Veeva Vault Safety, a range of resources are available, including blog posts, articles, case studies, and videos. These materials provide insights into optimizing safety data control, transforming pharmacovigilance practices, and leveraging safety intelligence to enhance patient safety.


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Streamlining Commercial Content Management with Veeva Vault PromoMats

Transforming the Content Lifecycle with PromoMats

Veeva Vault PromoMats is a comprehensive solution designed to streamline the end-to-end content lifecycle for commercial organizations. This regulated content management application facilitates the creation, review, and distribution of compliant content at scale. PromoMats covers various aspects of content management, including content creation, review and approval processes, digital asset management (DAM), claims management, and modular content development. By providing a unified platform for managing promotional content, PromoMats ensures efficiency and compliance throughout the content lifecycle.

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Revolutionizing Clinical Data Management with Veeva Vault

Introduction to Veeva Clinical Data Solutions

Veeva Clinical Data offers a comprehensive solution for modern trials, ensuring seamless and connected data flow across patients, sites, and sponsors. In today's clinical data landscape, the increasing complexity and volume of data can be overwhelming. Veeva Clinical Data applications are designed to simplify data collection and processing for all stakeholders involved in clinical trials.

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Optimize Quality Control Operations with Veeva Vault LIMS

Enhancing Quality Control with Veeva Vault LIMS

Veeva Vault LIMS offers a cutting-edge solution to modernize and optimize Quality Control (QC) operations in various industries. By leveraging Vault LIMS, organizations can streamline batch release testing, manage stability studies, and monitor environmental conditions efficiently. This innovative platform drives digital method execution, ensures adherence to specifications, and enables review by exception, thereby expediting the product release process. Through its advanced features, Vault LIMS promotes compliance by validating user qualifications from Vault Training, providing effective test method procedures from QualityDocs, and initiating lab investigations seamlessly through QMS for out-of-specification results.

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Empowering Faster and More Precise Commercialization with Veeva Compass Suite

Unparalleled Data Solutions for Modern Commercial Needs

Veeva Compass Suite revolutionizes the commercialization process by offering a comprehensive set of modern data products that cater to the complexities of today's therapies. The suite provides access to patient, prescriber, and national data in a manner that ensures accuracy, timeliness, and completeness. By leveraging Veeva Compass, organizations can accelerate their product launches, empower field teams with a holistic view of customers, and drive impactful decision-making.

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Enhancing Patient Experience in Clinical Trial Participation with Veeva Vault

Streamlined Access to Study Information

Veeva Vault offers a comprehensive solution to enhance patient experience in clinical trial participation. With MyVeeva for Patients, individuals have a single point of access for all study documents, actions, and communications. This streamlined approach ensures that patients can easily view study information, understand important details, and stay connected with their clinical site.

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