Veeva Connections | Veeva Systems Europe
Regulatory Connections
Connections
Section 1: RIM – Clinical Operations
RIM – Clinical Operations
Announced 2020
Status Mature
Customers 50-100
Drive more efficient collaboration between clinical and regulatory teams by sharing product, study, site and submission data along with investigator CVs, 1572s, protocols, and investigator brochures.
- Product and Study Data: Any RIM and Clinical – Sync study and product data across applications
- Document Exchange: eTMF and Submissions – Accelerate document readiness by automating availability in corresponding system
- Submission Tracking: SSU and Submissions – Automatically track submission data, reducing manual steps and reconciliation
Veeva Help
- Vault Help About the RIM-Clinical Operations Connection
- Vault Help Configuring the RIM-Clinical Operations Connection
- Vault Help Technical Details for Creating and Managing Veeva Connections
Customer Success Stories
Additional Resources
RIM – PromoMats
Announced 2021
Status Mature
Customers 11-50
Accelerate business operations by automating the management of documents and product data between Veeva RIM and Veeva PromoMats.
- AdPromo Submissions: Submissions and PromoMats – Link eCTD documents in PromoMats to Veeva Submission Content Plans
- Document Exchange: Submissions and PromoMats – Automate transfer of documents using document crosslinks from approved content
- Product Data: Any RIM and PromoMats – Sync product data to allow marketing teams make informed decisions
Veeva Help
Additional Resources
Quality – RIM
Announced 2019
Status Mature
Customers 11-50
Automate the coordination of product change control activities by sharing critical data and documents between the Quality (QMS) and Regulatory (RIM) Vaults, speeding up regulatory assessments and ensuring compliance.
- Product Data: Any Quality and RIM – Single source of truth for product data to ensure consistency and accuracy
- Enhanced Change Control: QMS and Registrations – Accelerate bidirectional change controls with regulatory impact seamlessly
- Document Exchange: Quality Docs and Submissions – Share documents across teams and eliminate redundant effort
Veeva Help
Customer Success Stories
Additional Resources
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
Veeva Help
Additional Resources
RIM – Medical
Announced 2026
Status Early
Customers 1-10
Accelerate medical workflows by centralizing your product and regulatory data. One source of truth for medical inquiries and document management to ensure compliance.
- Product Data: Any RIM and any Medical – Sync product data to increase compliance and efficiency
- Document Exchange: Submissions and MedComms – Automate document transfer to accelerate medical content workflows