Transforming Regulatory Intelligence

When forming a country-specific strategy for product development or commercialization or life cycle changes, you need right "Information and Intelligence" and not just "Data". As critical decisions depend on what you provide to your company/teams, this information should not only be accurate but dependable.

With constant regulatory changes globally, keeping track of these and staying on top is a real challenge. In addition to this, the volume of data growing daily mounts additional burden on Regulatory Professionals. Summarize from Vistaar is a collection of pre-compiled regulatory requirements for 112 countries reviewed manually.

HUNT from Vistaar is "AI driven" to help you do “Contextual” search of our repository consisting of over 1.2M regulations and guidance documents from global health authorities and government regulatory authorities which gets updated daily.

Depending on search engines or Health Authority websites is time consuming. In addition most of regulatory authorities constantly purge older documents making it tough for some of your projects involving wider and deeper regulatory documents. Leverage our AI based search to help you perform quick, insightful searches on thousands of documents

Whether you are planning a new poduct development or expanding your current product for new indications or patient population, Knowing “what’s out there” is one of the key initial steps. Label Intel helps you exactly doing that. With 215k approved labels (both drugs and devices) pre-loaded and updated daily, you can search by product or company or indications to find your baseline comparison labels. You can do side-by-side comparisons for effective analysis.

You can compare information such as drug exposure and clinical response variability, mechanisms of drug action, polymorphic drug target, genotype-based dosing, disposition pathways, risk for adverse events, precautions/alerts, drug–drug interactions, contraindications, and nutritional management across the medicines and medicinal products.

Advisory Playbooks acts as your guide or use to verify or as 2nd opinion of your initial plans driving initial probing questions, you can give your needs or plans in simple English. Vistaar by leveraging its AI engine enables you to frame a Regulatory & Clinical strategies by providing what is needed, options, country requirements, forms/checklists, similar competitive product lables, related clinical trials, what other companies are doing in that scenario, and more.

Keeping up to date with required standards is key for medical devices to be compliant in different countries. As standards are developed by several agencies/bodies, keeping track of all the associated questions as who’s updating and what is being updated has always been a manual and time-consuming task. VISTAAR Standards module keeps you current on the standards on each and every update along with the current versions with extensive details.

RegBot with its chat interface gets you information faster for your simpler questions. “Always on”, this chat application saves your time in searching and gets simpler answers faster by using AI techniques at the backend.