Regulatory Intelligence, Monitoring and impact management Platform
Manage your Regulatory Requirements effectively
With our regulatory intelligence software, you can confidently stay up to date with the latest regulatory requirements applicable to your organization. Vistaar streamlines classification, organization, and impact assessment of regulations while ensuring centralized monitoring without the hassle of spreadsheets or multiple systems. Receive real-time regulatory alerts, guidance, and standards throughout the product life-cycle process to ensure compliance.
Smart Library
Gain access to a vast regulatory intelligence database covering global regulations in multiple industries, including biopharma, medical devices, digital health, consumer health, OTC, food, and cosmetics.
Organize content & data by applicable topics, access document summaries, and create tasks to prioritize high-risk items.
Stay updated with manually reviewed regulatory changes and receive summarized updates from Vistaar.
Monitoring & Alerting
Vistaar continuously monitors market- and product-related regulations specific to your needs.
Receive only relevant regulatory alerts, filtering out unnecessary information for a clear, at-a-glance view of critical updates.
Utilize our automatic change-tracking feature to quickly identify and review regulatory modifications in a streamlined process.
Intelligent Search
Leverage regulatory intelligence solutions to help your team quickly adapt to internal and external changes, including entering new markets or expanding geographically.
Access millions of regulatory and guidance documents across hundreds of countries with our AI-powered search engine, linking regulations to applicable products.
One Comprehensive Regulatory Intelligence Platform
Bring regulatory, labeling, clinical, quality, and compliance teams together on a single regulatory intelligence software solution, eliminating fragmented activities and multi-versioned spreadsheets.
Ensure cross-functional alignment and automate time-consuming, labor-intensive tasks, allowing teams to focus on high-priority projects.
Access translated guidance documents and timely alerts to ensure compliance with evolving regulations.
Leverage a 2-million-document repository of global health authority regulations and guidance, updated daily, and searchable using AI-driven technology.
Utilize software that manages the full regulatory cycle—from monitoring to alert review, global impact assessments, and next steps.
Enjoy built-in project management functionality and cloud-based intuitive tools.
Access regulatory intelligence pharma and regulatory intelligence medical device insights with country-specific translations within the tool.
Optionally, combine with our expert consulting services for specialized projects requiring additional expertise.
Monitor global clinical trials through aggregated global registry data to track ongoing clinical activities.
Seamlessly integrate with your existing systems to incorporate regulatory intelligence into daily operations.
With this regulatory intelligence platform, you can ensure streamlined compliance, proactive regulatory monitoring, and efficient management of global regulatory requirements – all in one powerful solution.
