Transforming Regulatory Intelligence
Information You Need To Make Critical Regulatory &
Compliance Decisions
Summarize (Regulatory Summaries)
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.
Key Benefits:
- Best pricing in the industry guaranteed with flexible (Pay by country, business area, month, year, user) options
- Get covered on all regulatory requirements (pre R&D to Life Cycle). View Sample Report of BioPharma or Medical Device
What’s Included & Value !
A single comprehensive regulatory requirements database. Regulatory requirements reports enable Pharma, Biotech, Consumer Health 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
Features:
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 112 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 (Health Authority documents repository)
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
"Authoritative" Regulatory Documents in ONE place and in ONE search
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
- Hundreds of Daily updates added to our repository of Million+ documents
- Saves time drastically with great accuracy
- Intelligent AI based search
- All countries in 1 location
- Don’t bother saving these large documents and maintaining them
Be sure about the documents. Save your time. Improve your productivity.
Advisory Playbooks (Guide for planning Strategies)
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.
Your Benefits
- Cut endless hours of time spent, with no guarantee of finding what you want, on search engines (or blogs or magazines or news letters)
- You can know what’s happening, why it’s happening and how to respond
- Keeps you gain insight into what proactive steps can be taken
- For just few answers you can get entire clinical, product and regulatory intelligence information to plan your strategies in an efficient manner
Standards (Quality Standards for Med Device companies)
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
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.
