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Clinical Data Management

Collect and verify site data

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Veeva Site Connect

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Clinical Operations

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Manage trials end-to-end

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VEEVA Development Cloud

Vault Registrations

Track global registrations

Vault Submissions

Plan and manage submissions

Vault Submissions Publishing

Publish to health authorities

Vault Submissions Archive

Access submissions history

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Manage global quality processes

Vault Product Surveillance

Simplify postmarket surveillance for medical devices

Vault QualityDocs

Improve quality and compliance

Vault Validation Management

Manage and execute paperless validation

Vault Station Manager

Enable shop floor efficiency

Automate training management

Optimizing QC labs for real-time batch release

Accredited GxP eLearning Courses

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VEEVA Development Cloud

Mitigate risk with oversight

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Manage safety content

Vault Safety.AI

Automate case intake with AI

Manage signals from detection through risk evaluation and mitigation

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Veeva Medical Suite

Engage stakeholders across channels

Real-time customer intelligence

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Scientific content and inquiry management

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VEEVA Commercial Cloud

Data

Customer Reference Data

Delivers accurate data, faster

Master Data Management

A single, customer master record

Real-time customer intelligence

U.S. prescription and medical claims data

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Data science and analytics platform

Crossix Marketing Analytics

Marketing measurement, targeting & insights

Engagement

Multichannel CRM

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Events Management

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Content

Review & Approval + DAM

Compliant content and digital assets

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Master your multicenter studies

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Submissions Archive

Quickly access submissions history

Improve adherence & compliance

Global process management

Product Surveillance

Simplify post-market surveillance

Streamline training & ensure compliance

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End-to-end content management

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September 9, 2021

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October 14, 2021

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November 18, 2021

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