Clinical Operations Connections
Clinical Operations – EDC
Announced 2021 Status Mature Customers 50-100
Eliminate transcription errors, duplicate data entry, and separate logins by automating data transfer between clinical data management and clinical operations teams.
- Study Data: CTMS and EDC-Sync study data across applications.
- Subject Tracking: CTMS and EDC-Real-time visibility of enrollment and patient status.
- Enhanced Monitoring: CTMS and EDC-Simplified monitoring, including planning, conduct, and reporting.
- Protocol Deviation Management: CTMS and EDC-Track protocol deviations in CTMS that are detected and created in Clinical Data.
- Site Payments: Payments and EDC-Automatically trigger payable items based on procedures.
- Final CRF: eTMF and EDC-Automatically share final case report forms with the Trial Master File.
Clinical Operations – Medical CRM
Announced 2022 Status Early Customers 1-10
Improve the HCP experience by coordinating efficiently between clinical and medical teams. Enables transparency of clinical activities for medical, and medical interactions for clinical teams by automating data transfer data between Clinical Operations (CTMS) and Veeva CRM.
- Study Data: CTMS and Medical CRM (Veeva CRM)—Sync study data across applications.
- Activities and Interactions: CTMS and Medical CRM—Enable transparency of HCP interactions across clinical and medical teams.
Additional Resources
eCOA – Clinical Operations
Announced 2023 Status Early Customers 1-10
Streamline study start up and close out procedures with study and eCOA data alignment.
- Study Data: CTMS and eCOA—Provide a single source of truth for study, country, and site data.
- End of Study Media: eTMF and eCOA—Automatically transfer compiled eCOA data to Clinical Vault upon site lock.
RTSM – CDB
Announced 2024 Status Early Customers 1-10
Speed aggregation and cleaning of patient data by connecting RTSM with CDB.
- RTSM Data Extract: RTSM and CDB—Speed aggregation and cleaning of patient data.
RTSM – Clinical Operations
Announced 2025 Status Early Adopters Customers 1-10
Rely on Clinical Operations to be your single source of truth for core study data across Veeva Applications.
- Study Data: RTSM and any Clinical Operations—Sync study data across applications.
Additional Resources
RTSM – EDC
Announced 2023 Status Early Customers 11-50
Simplify subject and randomization data management.
- Subject and Randomization Data: RTSM and EDC—Automatically share subject-related data with EDC.
Additional Resources
Quality – Clinical Operations
Announced 2023 Status Early Customers 1-10
Automatically share clinical core study data with quality teams and streamline management of clinical trial issues.
- Study Data: Any Clinical Operations and any Quality—Provide a single source of truth for study, country and site data.
- R&D Issue Management: QMS and CTMS—Track GCP Deviations in QMS automatically by receiving Clinical Trial Issues from CTMS.
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.
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Customer Success Stories
Additional Resources
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.