Regulatory Intelligence, Monitoring and impact management Platform
Manage your Regulatory Requirements effectively
With our Regulatory intelligence solution, you will always be confident that you have the latest regulatory requirements that applies to your organization — whatever the country is. Streamline the process of classifying regulations, organizing them, and identifying impending changes, impact assessments, effective centralized monitoring without switching between spreadsheets or different systems. Continue to receive relevant regulatory alerts or guidance or standards throughout the entire legislative process, never missing a beat.
Smart Library
Get access to our large online database that provides you with global regulations in several industries (BioPharma, Medical Devices, Digital Health, Consumer Health, OTC, Food and Cosmetics)
Organize your library by applicable topics, get document summaries, and create tasks around them to prioritize high-risk items
When regulation changes, get alerted with the summary of changes manually performed by our analysts and experts
Monitoring & alerting
Let system monitor what you need and your market/product related information
Our platform will only send you alerts that apply to your organization directly, filtering out the noise and giving you an at-a-glance overview of what’s important
See exactly what’s new in the modified text with our automatic change-tracking feature and quickly identify the requirements that apply in one clean, easy process
Intelligent Search
Help your team to scale and quickly adapt to any internal and external changes, like entering new markets or expanding into new geographies, with Vistaar’s regulatory search capabilities
Get access to millions of Regulatory/Guidance documents across the globe in hundreds of countries at your fingertips, so that you can search for new regulations with ease using our AI powered search engine and link them to applicable products
One Regulatory Intelligence Platform
Have your regulatory, labeling, clinical, quality and compliance teams on one single platform, eliminating siloed activities and multi-versioned spreadsheets
Get everyone on the same page and automate time-consuming, labor-intensive tasks across the board, creating more room for high-priority work
Capabilities & your Benefits:
Manually reviewed regulatory summaries covering clinical, technical, QMS/Quality, market launches, testing standards, submission checklists, fees, labeling, import/export, marketing, safety/Vigilance, standards, life cycle requirements, and many more areas in a granular manner
Translated Guidance documents and timely alerts
Standard repository and monitoring to always be on top of upcoming changes
Over 2 Million Global regulatory document repository of health authorities’ regulations and guidance, updated daily and provided to you with AI-enabled search for faster and better match
Software to manage full cycle activity from monitoring to alerts review to share/assign to members, perform global impact assessment and finalize next steps
Full project management functionality included as standard functionality
Cloud based with intuitive easy-to-use tool
Country translations handled with in the tool
If needed, combine with our Services for any of your projects that need our team’s time or expertise
Global clinical trials gathered from global registries for you to see all clinical activity
Integrate with any of your existing tools to get this “knowledge” into your daily systems
