
Veeva Vault Study TrainingVeeva Systems
Veeva Vault Study Training is a robust solution designed to streamline and automate the training processes for clinical trials.
Vendor
Veeva Systems
Company Website

Product details
It unifies learning management and clinical operations, ensuring efficient and compliant training for research sites, CROs, and sponsor personnel.
Key Features
- Comprehensive Training Management:
- GCP and Study-Specific Training: Manages Good Clinical Practice (GCP) and study-specific training requirements, ensuring all personnel are adequately trained.
- Diverse Training Formats: Supports various training formats, including documents, videos, SCORM/AICC modules, quizzes, and classroom sessions, tailored to specific curricula and training needs.
- Automated Processes:
- Role-Based Training: Automatically assigns training based on a user’s role and location, ensuring relevant and timely training for all team members.
- Protocol-Specific Curriculum: Allows the creation of protocol-specific training curricula, which are automatically assigned and tracked.
- Integration and Connectivity:
- Vault eTMF Integration: Connects with Vault eTMF to eliminate the need for manual capture of study and site information, ensuring real-time inspection readiness.
- Unified Reporting: Provides unified reporting across sponsors, CROs, and sites, improving oversight and compliance.
- Compliance and Inspection Readiness:
- Automated Documentation: Automatically documents completed training in an inspection-ready format, making it easy for study teams and Clinical Research Associates (CRAs) to access and leverage.
- Training Certificates: Automates the creation and filing of training certificates, ensuring ongoing compliance and readiness for inspections.
- Enhanced User Experience:
- On-Demand Content: Offers on-demand training content and automated alerts to ensure compliance and keep study teams informed.
- Real-Time Visibility: Provides real-time visibility into training status and compliance, helping to manage and track training activities effectively.
Benefits
- Increased Efficiency: Reduces the time and effort required to assign, deliver, and record study training, allowing CRAs and Clinical Trial Coordinators (CTCs) to focus on other critical tasks.
- Improved Compliance: Ensures that all training processes meet regulatory standards, reducing the risk of non-compliance.
- Better Oversight: Enhances oversight of study partners through unified reporting and real-time visibility into training activities.
- Streamlined Operations: Simplifies training management by consolidating all training activities into a single, easy-to-use platform.
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