Clinical, Regulatory, and
Quality for Emerging Biotech
Standardized, pre-configured Vault applications without the implementation and maintenance costs.
Announced 2024 | Status Early | Customers 1-10
Vault Quality
QualityDocs and Training
QualityDocs Basics is the industry-leading regulated quality content management solution. Including best practices for managing SOPs and other regulated content.
Vault Training Basics is an industry-specific LMS ensuring that your team is ready to perform their jobs while enabling GxP compliance and audit readiness.
Vault RIM
Submissions and Submissions Archive
Vault Submissions Basics is used to plan, collaboratively author, review, and approve regulatory documents. It includes dashboards and reports to allow submission managers to track the status of documents in real time.
Vault Submissions Archive Basics is a secure repository of submission-published output and includes a viewer for easy access to historical applications submitted to health authorities.
Vault Clinical
eTMF
Vault eTMF Basics is the leading trial master file application used to ensure quality, timeliness, and completeness of a TMF. It provides full content management capabilities for upload, version control, QC/approval, and real-time co-authoring for study documents.
Vault Basics
Industry-leading Veeva Vault with zero implementation
Best of breed Vault applications now pre-configured and pre-validated to be up and running quickly and easily.
Global Support & Training
End-user 24x7 support provided by the Veeva Global Support Center. Robust on-demand training for each application available just a click away.
Pre-Validated
Access complete validation packages on-demand, with every release pre-validated by Veeva. Conduct self-service vendor audits instantly.
Always Current
Veeva-managed updates, delivered three times a year, keep your Vault current and ensure you benefit from the latest features.
Powered by Veeva Vault
Built for Emerging Biotech, Managed
and Maintained by Veeva
"Veeva Vault Basics delivers the complete, pre-validated solution that we need to operate quickly and efficiently as we scale our business."
Phil Adams
Director of IT, Longboard Pharmaceuticals
"Veeva’s deep experience and expertise shines through in the depth and capability of Vault Basics. The history Veeva has from more than 1,000 customers across more than a decade, results in us being able to deploy a best of breed system with zero implementation and maintenance costs."
Meghal Majmudar
Head of Regulatory Operations, Inozyme Pharma
"With Vault Basics, we gain a fully compliant and validated system that delivers the functionality we need to easily author and manage quality documents including training, without lengthy implementation timelines."
Melissa Thompson
Director of Quality Assurance, NextPoint Therapeutics
"As a fast-growing biotech, we needed a predictable and compliant regulatory solution that could easily scale as the business changes. Veeva Vault Basics gives us a complete solution that will always be current so our teams can author and assemble submissions quickly and confidently."
Joanna Sambor
Head of Regulatory Affairs, Maplight Therapeutics
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Veeva Vault Basics
Let us know if you are interested in learning more about Veeva Vault Basics.