Vistaar
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About
Vistaar provides global regulatory, quality, labeling, safety, clinical, and compliance requirements for Pharma/Biotech, Devices, Diagnostics, OTC, Consumer Health, Cosmetics, and Digital Health domains. It combines smart technology and subject experts to deliver up-to-date regulatory updates and trusted insights accurately and faster, including translated guidance documents, all at a competitive price point. The platform covers 150+ countries' requirements, 2 million+ regulations & guidance documents, 1000+ standards monitoring, and 750k clinical trials. DDi acquired the Vistaar knowledge base in 2013 and added newer technology, including artificial intelligence, to make this knowledge easily accessible and affordable to users worldwide.
Platform
Features
• avoid being caught off-guard by frequent regulatory changes
• increase accuracy and timeliness of regulatory and compliance updates
• stay on top of important regulatory developments
• get digital centralized library of applicable regulations
• automate time-consuming tasks to save up to 70% on process reviews
• reduce noise with smart, configurable alerts for regulatory changes
• create a traceable matrix of laws, regulations, and guidance
• gain operational visibility and optimize processes
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