Software for Global Regulatory
VISTAAR provides Global Regulatory, Clinical and Compliance Requirements to Biopharma, Devices, Consumer Health, Cosmetics, and Digital Health. With a unique combination of smart technology and subject experts, you will get up to date requirements and trusted insights accurately and much faster. Over many years, VISTAAR has built deep data sets to help you do the right strategy. All this is done at the best price point in the industry.
Several times you wished for more hours in a day. If you have a lot of hours/time & spending that on search engines, you probably may get your data/answers. But your teams and company need data NOW.
VISTAAR normalized and structured over 160 data points for different scenarios spanning Drugs, Devices, Biologics, Consumer Health, OTC, Digital, and more.
All data are nicely organized vertically and cross-sectional by Manufacturing/CMC, Clinical, Testing, Packaging & Labeling, Registration, Submissions, Safety & Vigilance, Standards, Compliance, and more.
In addition to these, our AI and Technology helps to get what you want, FASTER.
Cost Effective
Finding it tough to put $$ value to “Knowledge”?
Intelligence and Insights, in some companies, are seen as nice-to-have but you know well, that’s must-to-have.
So we made it easy for you by making this COST EFFECTIVE. By leveraging “technology” and reducing operational “waste”, we accomplished this.
Try before you Buy.
Depth & Breadth
Your time should be spent on “Analysis & Decisions” rather than “search & searching”. Don’t you agree?
Growing business demands, therapeutic and product development complexities pose multi-faceted questions. Data covering different countries, various types, multiple contexts are needed to answer these questions for you to form the right strategy.
VISTAAR collects, curates, classifies several datasets using technology and our subject experts so that each question is answered holistically, covering different data sets.