AI Tool

Streamline Your Regulatory Submissions with Veeva Vault

End-to-end management of eCTD submissions on a unified cloud platform.

Maximize efficiency with automated workflows and interactive dashboards.Ensure regulatory compliance with robust audit trails and support for eCTD standards.Foster collaboration with Microsoft Office integration for seamless authoring.

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VerticalsLife SciencesRegulatory Submissions
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overview

Comprehensive Submission Management

Veeva Vault Submissions offers an all-in-one solution to manage the entire regulatory submission lifecycle. From planning and authoring to review and publishing, our cloud platform enhances transparency and efficiency for regulatory teams.

  • Single unified platform for all submission processes.
  • Real-time status updates to keep stakeholders informed.
  • Powerful tools to identify and resolve bottlenecks swiftly.

features

Key Features for Regulatory Teams

Our suite is designed to address common challenges faced by regulatory teams, facilitating effortless collaborative efforts and ensuring compliance across multiple markets.

  • Auto-matching and rules-based publishing integration.
  • Multi-user editing capabilities with Microsoft Office.
  • Support for global regulatory standards and workflows.

use_cases

Ideal for Life Sciences Organizations

Veeva Vault Submissions is tailored for life sciences companies managing complex, multi-market regulatory requirements. It streamlines submissions while maintaining compliance across diverse regions and regulatory standards.

  • Extensive support for eCTD standards.
  • Centralized content reuse for efficiency.
  • Robust audit trails for transparency and accountability.

Frequently Asked Questions

What is Veeva Vault Submissions?

Veeva Vault Submissions is a cloud-based RIM suite that facilitates the planning, authoring, review, approval, and publishing of eCTD submissions.

How does Veeva Vault improve efficiency?

With automated workflows and real-time dashboards, Veeva Vault helps users track submission progress and quickly identify and address any bottlenecks.

Is Veeva Vault Submissions suitable for global use?

Yes, it supports extensive eCTD standards and market-specific workflows, making it ideal for life sciences organizations that need to comply with diverse regulatory requirements.