by Veeva Systems
Enables seamless inbound and outbound engagement for sales and service teams within life sciences through CRM-integrated call center capabilities.
Collaboration & Knowledge Sharingby Veeva Systems
Generates compliant electronic submissions for global health authorities, integrating content plans and direct submissions from Vault.
Regulatory & Quality Complianceby Veeva Systems
Cloud-based system for managing life sciences quality processes such as CAPA, audits, and supplier management globally and in real time.
Regulatory & Quality Complianceby Veeva Systems
Comprehensive, quarterly data on HCP access metrics for improved segmentation and targeting in the life sciences.
Collaboration & Knowledge Sharingby Veeva Systems
A clinical database for aggregating, cleaning, and transforming clinical trial data from multiple sources into a unified format for analysis.
Clinical Trial Managementby Veeva Systems
Manages pharmacovigilance-related content and processes including PSMFs, PVAs, reports, literature review, and safety signal investigations.
Regulatory & Quality Complianceby Veeva Systems
An electronic investigator site file simplifies management of regulatory documents, enabling compliance and efficient monitoring for clinical trial sites.
Regulatory & Quality Complianceby Veeva Systems
A CRM for life sciences teams to enhance scientific engagement and manage customer relationships efficiently.
Collaboration & Knowledge Sharingby Veeva Systems
Manages start-up activities of clinical trials including feasibility, qualification, and activation of research sites.
Clinical Trial Managementby Veeva Systems
Enables electronic Clinical Outcome Assessments for trials, managing data from patients, clinicians, and caregivers via an app or web interface.
Clinical Trial Managementby Veeva Systems
Streamlines management of postmarket incident reporting for medical devices, enhancing safety, reliability, and quality.
Regulatory & Quality Complianceby Veeva Systems
End-to-end solution automating batch data aggregation, reviews, and traceability for streamlined GMP release decisions.
Regulatory & Quality Complianceby Veeva Systems
A platform for managing pharmaceutical event lifecycles, covering aspects like content, attendees, speakers, and expenses for different event types.
Laboratory Information Management System (LIMS)by Veeva Systems
A platform for managing the creation, approval, and distribution of promotional content in compliance with regulations.
Regulatory & Quality Complianceby Veeva Systems
Projected prescriptions and procedures data at various levels for 4,000+ brands in the U.S. market.
Collaboration & Knowledge Sharingby Veeva Systems
A reporting and analytics solution for simplifying advanced safety reporting and data analysis, leveraging Amazon Redshift for fast, consistent data updates.
Scientific Data Infrastructureby Veeva Systems
Provides accurate, compliant data on global investigators and sites with automatic updates for streamlined clinical trials.
Clinical Trial Managementby Veeva Systems
An LMS designed for GxP compliance, managing content creation, training plans, and compliance tracking.
Regulatory & Quality Complianceby Veeva Systems
A tablet app providing manufacturing operators offline access to relevant work instructions and procedures.
Bioprocess Development & Manufacturingby Veeva Systems
Provides a unified access point for patients to manage study documents, communications, appointments, and tasks, enhancing their clinical trial experience.
Clinical Trial Management