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.

    • 120+
    • Countries Requirements
    • 1.2M
    • Regulations & Guidances
    • 750k
    • Clinical Trials
    • 250k
    • Marketed Product Details
    • 50+
    • Product Environmental Compliance Requirements

Why VISTAAR?

Industries we serve

    • BioPharma
    • 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...
    • Cosmetics
    • 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

Monday, February 22, 2021

Labeling and IFU Compliance Soon to Follow EU MDR...

Multiple manufacturers are seeing postponement of...

Monday, February 22, 2021

EU Regulations: Things Still to be known

Medical Device Regulations (EU) 2017/745 is an...

Friday, January 29, 2021

Clinical Intelligence for better Clinical Trials

Every sector including healthcare is based on...