Intake to Insight on a
Unified Safety Platform
Case processing, signal detection, advanced reporting, and
safety content management.
UCB Unifies Global Pharmacovigilance Operations with Veeva Safety Suite
Veeva Safety Suite
Safety Suite of applications operate as a unified pharmacovigilance system on a single cloud platform to maximize operational efficiencies and improve patient safety.
Safety applications share a common data model which enables the end-to-end management of safety processes.
Veeva Safety
Global safety case intake, processing, and ICSR reporting.
Veeva SafetyDocs
Safety / pharmacovigilance-related content and process management.
Veeva Safety Workbench
Reporting and analytics application that requires Veeva Safety.
Veeva Safety Signal
Signal detection application that requires Veeva Safety.
Veeva AI for Safety
See in Action
“The technology becomes a key enabler to being able to work more effectively and enabling our pharmacovigilance colleagues to do the things that they get excited about.”
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Cory Gilbert
Senior Director, PV Operations & Global Process Enablement
“With a single collaborative safety platform, we can standardize terminology, increase data quality and accessibility, and improve communications to health authorities.”
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Adrian Maynier
Head of Systems
“Our partnership with Veeva allows us to stay at the forefront of technological advancements in the industry. We are now streamlining our operations and improving efficiency.”
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Bonne Adams
Vice President, Operations
Veeva Connections
Veeva Connections are Veeva-delivered integrations that seamlessly transfer data and documents.
Safety-EDC Connection
Automates flow of clinical serious adverse event (SAE) data, and provides safety teams direct access to subject data.
Safety-Clinical Operations Connection
Enables seamless flow of safety letters to Veeva eTMF, and with CTMS and SiteConnect, distribution to sites with tracking.
Medical-Safety Connection
Streamlines intake of adverse event data from medical.
Safety–RIM Connection
Shares registered product data.
See a full list of available Veeva Connections.
What PV Teams Need to Know for FDA E2B(R3)
Understand the FDA E2B(R3) reporting requirement for serious and unexpected suspected adverse reactions (SUSARs) and discover what PV teams need to do to prepare.
