What we do

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.

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    • 150+
    • Countries Requirements
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    • 1.4m
    • Regulations & Guidances
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    • 750k
    • Clinical Trials
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    • 371k
    • Marketed Product Details

How Vistaar works

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Vistaar automates heavy manual processes using Automation & artificial intelligence (AI) to help you manage regulatory change and compliance proactively and ensure timely mitigation in your organization. End-to-end Digital design automates and simplifies data acquisition, transformation, reporting and sharing .

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Global Resources

Our global team of Analysts and Subject Experts, with expertise across a diverse range of industries, geographies and policy areas, collaborate with functional specialists to address questions about regulations including purpose, applicability, requirements highlights and more. All reports are vetted to ensure data and summaries are accurate and up-to-date.

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Value to you
  • Improve Regulatory Foresight

  • Cut down Alert Noise

  • Unifying UI for full coverage of Regulatory value chain

  • Data & workflow Automations to reduce manual work

  • Lower Total cost of Ownership (TCO)


From the Blog


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