Veeva Development Cloud Services
Comprehensive implementation and consulting services for Veeva's R&D platform, helping pharmaceutical companies streamline clinical, regulatory, quality, and safety operations.
Veeva Development Cloud by IntuitionLabs
Veeva Development Cloud is the industry's leading unified platform for life sciences R&D, encompassing clinical, regulatory, quality, and safety operations. IntuitionLabs specializes in helping pharmaceutical and biotech companies implement and optimize these solutions to accelerate drug development while ensuring compliance.
Our Development Cloud Services
We offer comprehensive implementation and optimization services across the Veeva Development Cloud suite.
- Clinical Suite Implementation: Full-service implementation of Veeva Vault eTMF, CTMS, EDC, and other clinical applications with data migration and validation.
- Regulatory Information Management: Implementation of Vault RIM for managing drug registration data, health authority submissions, and IDMP compliance.
- Quality Management: Deployment of Vault QualityDocs, QMS, and LIMS for GxP document control and quality processes.
- Safety & Pharmacovigilance: Implementation of Vault Safety for adverse event case management and safety document control.
- Integration Services: Connect Development Cloud with other enterprise systems using Veeva APIs and custom connectors.
- AI-Powered Enhancements: Custom AI solutions for document classification, metadata extraction, and predictive analytics.
Clinical Suite Implementation
End-to-end implementation of Veeva Vault eTMF, CTMS, EDC, and other clinical applications. We handle data migration, validation, and compliance documentation for regulated environments.
Regulatory Information Management
Implementation of Vault RIM for managing drug registration data, health authority submissions, and IDMP compliance. We ensure your regulatory operations meet global requirements.
Quality Management
Deployment of Vault QualityDocs, QMS, and LIMS for GxP document control and quality processes. We help you establish a unified quality management system.
Safety & Pharmacovigilance
Implementation of Vault Safety for adverse event case management and safety document control. We ensure your safety operations meet global pharmacovigilance requirements.
Our Development Cloud Service Offerings
Comprehensive services to support your Development Cloud journey from implementation to optimization.
Clinical Suite Services
Implementation, migration, and AI-powered enhancements for Veeva Vault eTMF, CTMS, EDC, and other clinical applications.
Learn moreRegulatory Suite Services
Implementation of Vault RIM for managing drug registration data, health authority submissions, and IDMP compliance.
Learn moreQuality Suite Services
Deployment of Vault QualityDocs, QMS, and LIMS for GxP document control and quality processes.
Learn moreSafety Suite Services
Implementation of Vault Safety for adverse event case management and safety document control.
Learn moreIntegration Services
Connect Development Cloud with other enterprise systems using Veeva APIs and custom connectors.
Learn moreAI-Powered Enhancements
Custom AI solutions for document classification, metadata extraction, and predictive analytics.
Learn moreOur Approach to Development Cloud Services
Life Sciences Focus
Deep expertise in pharma and biotech R&D processes, with specialized knowledge in regulated content management and clinical operations.
AI-First Solutions
Leverage cutting-edge AI to enhance Development Cloud solutions with predictive analytics, automation, and intelligent insights.
Compliance by Design
All solutions are built with regulatory compliance in mind, including GxP, FDA 21 CFR Part 11, and EU Annex 11 requirements.
Veeva Development Cloud: Frequently Asked Questions
Ready to Transform Your R&D Operations?
Contact IntuitionLabs to discuss how we can help you maximize your Veeva Development Cloud investment with expert consulting, implementation, and AI-powered enhancements.
Schedule a Consultation