Vistaar

Vistaar is a regulatory intelligence platform designed for pharmaceutical, medical device, digital health, consumer health, OTC, food, and cosmetics companies. It supports regulatory, labeling, clinical, quality, and compliance teams in monitoring, classifying, and assessing the impact of global regulations across the full product lifecycle, replacing fragmented spreadsheets and disconnected systems with a single centralized solution.

The platform covers the complete regulatory cycle — from initial monitoring and alert review through to global impact assessments and next steps — and includes built-in project management tools delivered via a cloud-based interface.

Smart Library

• Provides access to a regulatory intelligence database covering global regulations across biopharma, medical devices, digital health, consumer health, OTC, food, and cosmetics industries.
• Allows users to organize content and data by applicable topics, access document summaries, and create tasks to prioritize high-risk items.
• Delivers manually reviewed regulatory changes with summarized updates to keep teams current.

Monitoring and Alerting

• Continuously monitors market- and product-specific regulations based on each organization's needs.
• Filters regulatory alerts to surface only relevant updates, providing a clear view of critical changes.
• Includes an automatic change-tracking feature to identify and review regulatory modifications efficiently.

Intelligent Search

• Provides an AI-powered search engine covering millions of regulatory and guidance documents across hundreds of countries.
• Links regulations directly to applicable products, supporting teams adapting to internal changes such as new market entry or geographic expansion.

Cross-Functional Collaboration

• Brings regulatory, labeling, clinical, quality, and compliance teams onto a single platform, eliminating fragmented workflows and multi-versioned spreadsheets.
• Supports cross-functional alignment and automates time-consuming, labor-intensive tasks so teams can focus on higher-priority work.

Capabilities and Document Coverage

• Manually reviewed regulatory summaries covering clinical, technical, QMS/quality, market launches, testing standards, submission checklists, fees, labeling, import/export, marketing, safety/vigilance, and lifecycle requirements.
• Access to translated guidance documents and timely alerts for evolving regulations.
• A repository of approximately 2 million global health authority regulations and guidance documents, updated daily and searchable via AI-driven technology.
• Country-specific translations available within the tool for pharma and medical device regulatory intelligence.
• Global clinical trial monitoring through aggregated global registry data to track ongoing clinical activities.
• Built-in project management functionality alongside cloud-based tools.
• Optional combination with expert consulting services for specialized projects requiring additional expertise.

Vistaar integrates with existing organizational systems to incorporate regulatory intelligence into daily operations. It is part of a broader product suite that includes REGai, mIRT, TULA, and smartDOC, developed by DDi.