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Connections

Clinical Operations Connections

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Clinical 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 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 – DQS

Speed aggregation and cleaning of patient data by connecting RTSM with DQS.
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

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eCOA – 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 – DQS

Speed aggregation and cleaning of patient data by connecting RTSM with DQS.
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

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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.
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

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Safety – 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

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Quality – 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

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Medical – 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 – Vault 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.

Medical – Vault CRM

Connect upstream scientific communication to downstream engagement with compliant content sharing and seamless coordination between medical information and field teams.

PromoMats – Vault CRM

Empower your field teams by ensuring they have automated access to the latest CLM content in Vault CRM, along with the necessary data to sort and filter.

Medical – Network

Simplify medical inquiry contact lookup by searching for the HCP’s contact information in your reference data without leaving MedInquiry.

Medical – Quality

Streamline product quality complaint (PQC) intake and case processing by automating the flow of complaint records between MedInquiry and QMS.

RIM – Medical

Eliminate process silos with a single source of truth for product data and labeling content, accelerating medical tasks with high reliability on regulatory data.