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 over 112+ countries reviewed manually.
A single comprehensive regulatory requirements database. Regulatory requirements reports enable Pharma, Biotech and Medical device companies understand and efficiently manage the demanding complexity of the varied regulatory requirements to plan/manage their products in various markets.
These are a big time-saver for you. The module features extensive information on all aspects (pre R&D to Life Cycle data) of Drugs, Biologics, Generics, Medical devices & Diagnostics
Clear & Concise
Our unique Regulatory Intelligence platform uses advanced technology to provide dependable information that cuts through the complexity and sheer volume of content within the regulatory compliance environment. Depending on the granularity based on your needs, you can utilize intuitive search and interface to review as well as download what you want.
Breadth & Depth
Covers over 100+ regulatory bodies from regulated and semi regulated countries. Authentic regulatory summaries retrieved from authority websites and reviewed by experts. Updated frequently, you can be rest assured on the "freshness" of the Intel.
VISTAAR provides precompiled manually reviewed regulatory summaries spanning advisory, clinical, IRB, market launches, testing standards, submission check lists, fees, labeling, import/export, marketing, safety/PV, life cycle requirements, and many more areas in a granular manner.
Cost & ROI
Transparent upfront costing options that you can mix/match to fit your needs. Best ROI in the industry, Guaranteed!!
HUNT from Vistaar is "AI driven" to help you do “Contextual” search of our repository consisting of over 980K 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
HUNT understands your queries in natural language and adjusting search results to potentially eliminate hours of browsing through the websites of health agencies or public search engines to get right regulations or guidance documents. Unlike other search engines, HUNT is built with AI-powered (NLP & ML) search capabilities for true regulatory search and requires no additional tuning.
Features & Benefits
Be sure about the documents. Save your time. Improve your productivity.
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 200k+ 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.