{"best_for":["Pharmaceutical companies","Biotechnology organizations","MedTech companies","Clinical research sites","Life sciences R&D teams"],"citation":{"dataset":"aitoolsforbusiness-agent-tool-export","directory_tool_url":"https://aitoolsforbusiness.ai/veeva","json_profile_url":"https://aitoolsforbusiness.ai/data/tools/veeva.json","markdown_profile_url":"https://aitoolsforbusiness.ai/data/markdown/tools-md-046.json","schema_version":"1.4.0","suggested_citation_label":"AI Tools for Business: Veeva (https://aitoolsforbusiness.ai/veeva)"},"features":["Veeva Vault Platform: A centralized cloud environment for managing industry-specific data, content, and AI agents.","Clinical Solutions: Tools for clinical trials, including eTMF for inspection readiness and CTMS for trial management.","Regulatory Solutions (RIM): Applications to plan, author, review, and approve regulatory documents and track global registrations.","Quality Cloud: Supports quality processes including GxP document control, QMS, and validation management.","Veeva AI: Agentic AI integrated into the Vault Platform to provide industry-specific assistance and support workflows.","SiteVault: Solutions for research sites to digitize study binders and track patient activity."],"freshness_status":"fresh","name":"Veeva","pricing_note":"SiteVault is free for research sites with up to 20 active studies. Pricing for larger sites is tiered. Buyers should confirm current pricing on the vendor website.","pricing_url":null,"primary_category":"Healthcare","profile_last_verified":"2026-06-05T14:12:41.289Z","secondary_categories":[],"short_description":"Veeva provides cloud-based software and data solutions for the global life sciences industry, supporting clinical, regulatory, and quality management.","slug":"veeva","sponsorship_status":"none","url":"https://aitoolsforbusiness.ai/veeva","use_cases":["Clinical Trial Management: Using CTMS and eTMF to track patient activity and maintain documentation.","Regulatory Submission Planning: Planning and authoring regulatory documents to manage submissions to health authorities.","Quality Process Centralization: Transitioning from paper-based or fragmented systems to a unified quality management system (QMS).","Pharmacovigilance: Managing the intake and processing of adverse events through a safety platform.","Digital Investigator Site Files: Digitizing study binders using eISF to support remote monitoring."],"website_url":"https://veeva.com/"}