What we do
VISTAAR provides Global Regulatory, Clinical and Compliance Requirements to BioPhrama, 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.
- Countries Requirements
- Regulations & Guidances
- Clinical Trials
- Marketed Product Details
- Product Environmental Compliance Requirements
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.
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.
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.
Industries we serve
- With growing patient safety emphasis and new product classes, all countries are actively changing or introducing regulations daily…
- Medical Devices
- Except for few markets, most countries med device regulations are either hazy or decentralized (decisions are distributed among several government offices) and you need a dependable source...
- Consumer Health
- Consumer Health requirements are more complex than BioPharma as its breadth is wide (OTC, food, cosmetics, and you name it..). But regulatory budgets are not on par like Biopharma...
- Though harmonization in regulations is increasing, still important differences are there for marketing or selling cosmetics in major markets. To overcome the hitches...
From the Blog
Labeling and IFU Compliance Soon to Follow EU MDR...
Multiple manufacturers are seeing postponement of...
EU Regulations: Things Still to be known
Medical Device Regulations (EU) 2017/745 is an...
Clinical Intelligence for better Clinical Trials
Every sector including healthcare is based on...