Leveraging Your Veeva Vault Investment, Upcoming Webinar Hosted by Xtalks

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In this free webinar, attendees will learn about a variety of technical and business considerations that are required when adding new capabilities to an existing Vault, such as configuration management, data management, change management and training.

When adding a technical capability to an existing platform, planning and business considerations potentially affect all users, not only the function to be supported by the new capability.

Daelight Solutions expert speakers Dan Wheeler, Founder and CEO, and Teresa Montes, Clinical Practice Lead, will host “Leveraging Your Veeva Vault Investment,” a free Xtalks webinar, on Thursday, November 4, 2021 at 1 PM EDT.

If you work in the life sciences, you are probably using Veeva Vault in some capacity because Veeva’s product line has expanded to offer many Vaults based on business function, including clinical, regulatory and quality. Within each Vault, Veeva has steadily expanded the functionality available to customers. For example, Vault Clinical began as an electronic Trial Master File (eTMF) solution, but now you can add a Clinical Trial Management System (CTMS), Study Startup, Payments and Site Connect in addition to Clinical Suite tools, such as Electronic Data Capture (EDC), Clinical Data Base (CDB) and Vault Coder. Each capability will require an additional investment, but economies can be gained considering life science companies need to manage many disparate technologies to do so.

When adding a technical capability to an existing platform, planning and business considerations potentially affect all users, not only the function to be supported by the new capability. Therefore, a holistic approach is required if this type of implementation is to succeed.

This webinar for life sciences research & development leaders will focus on some careful technical and business considerations required when adding additional functional capability into an existing platform — Veeva Vault — including:

  • Changes required to existing functionality (e.g., Expected Document List [EDL], Milestones and Document types)
  • Data management (e.g., Master Data, Reference Data and Data Governance)
  • Business Processes and standard operating procedure (SOP) documents that span functional groups
  • Training across business functions
  • Security Roles/Permissions
  • System downtime/environment management
  • System Governance

For more information or to register for this event, click here.

ABOUT XTALKS

Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars to the global life science, food and medical device community. Every year, thousands of industry practitioners (from life science, food and medical device companies, private & academic research institutions, healthcare centers, etc.) turn to Xtalks for access to quality content. Xtalks helps Life Science professionals stay current with industry developments, trends and regulations. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.

To learn more about Xtalks visit http://xtalks.com
For information about hosting a webinar visit http://xtalks.com/why-host-a-webinar/

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Sydney Perelmutter
Xtalks
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