Veeva
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Veeva Vault QualityOne helps companies improve efficiency, visibility and control in quality management with an easy-to-use, secure cloud solution that unifies processes, documents and data.
The Vault RIM Suite provides fully integrated regulatory information management (RIM) capabilities on a single cloud-based platform including submission document management, product registration management, health authority correspondence and commitments, submission archiving, and comes with fully integrated IDMP capabilities.
A cloud-based solution that establishes one global authoritative source for managing regulatory activities, product registration data, and the end-to-end submission development process.
Veeva Medical Suite is designed specifically fo medical teams, empowering them to foster meaningful nad personalized scientific dialogues informed by a complete view of each stakeholder.
Veeva SiteVault Free reduces administrative burden in clinical trials by replacing manual, paper-based processes so you can focus on your patients. Manage regulatory and source documents in a system that supports 21 CFR Part 11 and HIPAA requirements. Save time with built-in tools to capture electronic signatures, enable remote monitoring, certify copies, and view reports. SiteVault Free can be used for all studies, regardless of what technology your sponsors use, as well as the site file for investigator-initiated trials.
With a real-time view across clinical trial processes, Vault CTMS improves operational efficiency, streamlines collaboration, and enables faster, higher-quality trial execution.
Azumuta
Product Description
Veeva Reviews
Julia V.
Narratives Project Manager, Pharmacovigilence Risk Management- Process and ComplianceUser friendly System
Sivan P.
Too many options/tabs, not very intuitive
Vaibhav K.
CMC Scientist - Regulatory Affairs & Biotechnology ProfessionalComprehensive tool to sort and maintain database.
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