Safety Connections
Safety – Clinical Operations
Announced 2022 Status Early Customers 1-10
Streamline safety letter distribution by automating the availability of study data and documents between Veeva Safety and Veeva Clinical Operations.
- Study Data: Any Safety and any Clinical Operations – Provides a single source of truth for study and country
- Safety Letters: Safety and eTMF (for DocX), Site Connect – Reduces safety letter distribution effort with document connectivity
Safety – EDC
Announced 2024 Status Early Customers 1-10
Streamline case processing through automated flow of SAE event records from EDC to safety inbox, reducing the need for serious adverse event reconciliation
- Adverse Event Intake: Safety and EDC – SAEs sync automatically and case processors can access data to process cases faster
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Safety – RIM
Announced 2023 Status Early Customers 1-10
Share product and registrations data between regulatory and safety to streamline case processing.
- Product Data: Any Safety and any RIM – enable a single source of truth for product and registration data
Medical – Safety
Announced 2024 Status Early Customers 1-10
Streamline adverse event intake and case processing through automated flow of AE event records from medical inquiry to safety inbox.
- Adverse Event Intake: Safety and Medical Inquiry – Accelerate intake process by automating the transfer of Adverse Events
Quality – Safety
Announced 2025 Status Early Customers 1-10
Automate intake by sharing product quality complaint and adverse event (AEs) data between Veeva QMS and Veeva Safety.
- Product Quality Complaint Intake: Facilitate intake of PQCs that were originally submitted to Veeva Safety
- Adverse Event Intake: Streamline intake of AEs that were originally reviewed by Quality