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Global Regulatory Intelligence

Vistaar, a global regulatory Artificial intelligence platform, is specially designed for the right decisions, faster access to accurate and authoritative global regulation. It extracts new regulations, changes in guidance, new legislations, changes in regulatory policy and procedures from several health authority sources and classifies and clusters regulatory updates into applicable categories (Clinical, Marketing, Lifecycle, Manufacturing, Labeling, Safety and key areas) based on the inbuilt insights proprietary regulations.

Vistaar is a combination of Regulatory and Artificial intelligence (RI&AI) fully integrated to deliver “Intelligence” faster & cost effectively. It is customized to a product or a market and a unique suite for global regulatory information auto analysis. It extracts regulatory information by automatically classifying & clustering regulation to meet your business goals. At a click, it provides information about any change or alert about regulatory update to the company stakeholders.


Regulatory Chabot

AI based Medium brings latest regulation or policy summary for the given free text context.


Regulations Repository

AI mechanized solution, simplifies information gathering processes by providing reliable document references or repository for all your regulatory needs. Built with a simple to use interface and a global search for searching legislations, policies and documents.


Document Analyzer

Using AI algorithms, Vistaar classified general Regulatory & Clinical media, news and notifies all stakeholders how a policy impact on the company or product or on a market(s).

Why us

  • Vistaar reports on current trends, provides interpretation of regulatory policy or guidance to improve product decision making and key performance Indicators.
  • Maintains centralized repository for regulatory intelligence or policy documents.
  • Keeps life science professionals up to date with constantly changing/evolving regulatory environment with an easy access to continuously updated accurate regulatory information.
  • Increases RA productivity drastically.
  • Provides updated regulatory data from multiple sources for clinical submissions, market authorization, safety reporting, manufacturing, and other details.
  • With simple mechanisms Vistaar helps clients to navigate progressively complex and stringent regulatory requirements - global markets.
  • Decrease your Regulatory Intelligence costs by at least 50%.

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