Veeva Connections Resource Hub
Clinical Operations Connections
View All ConnectionsClinical Operations – EDC
Eliminate transcription errors, duplicate data entry, and separate logins by automating data transfer between clinical data management and clinical operations teams.
Clinical Operations – Medical CRM
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.
eCOA – Clinical Operations
Streamline study start up and close out procedures with study and eCOA data alignment.
RTSM – CDB
Speed aggregation and cleaning of patient data by connecting RTSM with CDB.
RTSM – Clinical Operations
Rely on Clinical Operations to be your single source of truth for core study data across Veeva Applications.
RTSM – EDC
Simplify subject and randomization data management.
Quality – Clinical Operations
Automatically share clinical core study data with quality teams and streamline management of clinical trial issues.
RIM – Clinical Operations
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.
Safety – Clinical Operations
Streamline safety letter distribution by automating the availability of study data and documents between Veeva Safety and Veeva Clinical Operations.
Clinical Data Connections
View All ConnectionseCOA – Clinical Operations
Streamline study start up and close out procedures with study and eCOA data alignment.
Clinical Operations – EDC
Eliminate transcription errors, duplicate data entry, and separate logins by automating data transfer between clinical data management and clinical operations teams.
RTSM – CDB
Speed aggregation and cleaning of patient data by connecting RTSM with CDB.
RTSM – EDC
Simplify subject and randomization data management.
Safety – EDC
Streamline case processing through automated flow of SAE event records from EDC to safety inbox, reducing the need for serious adverse event reconciliation.
Regulatory Connections
View All ConnectionsRIM – Clinical Operations
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.
RIM – PromoMats
Accelerate business operations by automating the management of documents and product data between Veeva RIM and Veeva PromoMats.
Quality – RIM
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.
Safety – RIM
Share product and registrations data between regulatory and safety to streamline case processing.
Safety Connections
View All ConnectionsSafety – Clinical Operations
Streamline safety letter distribution by automating the availability of study data and documents between Veeva Safety and Veeva Clinical Operations.
Safety – EDC
Streamline case processing through automated flow of SAE event records from EDC to safety inbox, reducing the need for series adverse event reconciliation.
Safety – RIM
Share product and registrations data between regulatory and safety to streamline case processing.
Medical – Safety
Streamline adverse event intake and case processing through automated flow of AE event records from medical inquiry to safety inbox.
Quality – Safety
Automate intake by sharing product quality complaint and adverse event (AEs) data between Veeva QMS and Veeva Safety.
Quality Connections
View All ConnectionsQuality – Clinical Operations
Automatically share clinical core study data with quality teams and streamline management of clinical trial issues.
Quality – RIM
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.
Quality – Safety
Automate intake by sharing product quality complaint and adverse event (AEs) data between Veeva QMS and Veeva Safety.
Commercial Connections
View All ConnectionsMedical – Safety
Streamline adverse event intake and case processing through automated flow of AE event records from medical inquiry to safety inbox.
PromoMats – Medical
Simplify document management and enhance collaboration between medical and promotional teams by automatically transferring steady-state documents and their anchors seamlessly between Vaults.
Clinical Operations – Medical CRM
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.
RIM – PromoMats
Accelerate business operations by automating the management of documents and product data between Veeva RIM and Veeva PromoMats.