Simplify Regulatory Strategy & Change Management

Get up-to-date Requirements. Save time. Be Compliant.

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Large, small/medium Pharma, Medical Device & Consumer Health companies

What we do

Vistaar provides Global Regulatory, Quality, Labeling, Safety, Clinical and Compliance Requirements to Pharma/Biotech, Devices, Diagnostics, OTC, Consumer Health, Cosmetics and Digital Health domains. With a solid combination of smart technology and subject experts, you will get up-to-date regulatory updates and trusted insights accurately and much faster (including translated guidance documents). All this is done at the best price point in the industry.

150+

Countries Requirements

2 million

Regulations & Guidance Documents

1000+

Standards Monitoring

750k

Clinical Trials

Ingredients

REGULATORY Database

How Vistaar works

Technology_Global-Resources_Value-to-you_Updated

Benefits

Oversight

Gain operational visibility and optimize processes
Create a traceable matrix of laws, regulations, and guidance to do better impact assessment when changes come in
Reduce the noise with smart, configurable alerts that target only those regulatory changes that affect you
Spend up to 70% less time on process reviews by automating time-consuming tasks

Risk Mitigation

Get digital centralized library that is comprehensive and covers all applicable regulations you need to be compliant with today and going forward
Stay on top of important regulatory developments that have direct impact on your products and organization
Increase accuracy and timeliness of your regulatory and compliance updates

Stay Ahead

Avoid being caught off-guard by frequent regulatory changes that could affect your products (both in R&D as well as market) and compliance programs
Know exactly what incoming regulatory changes apply to your organization and review internal Policies / Processes accordingly
Assign to teams and track the status of each important change/alert
Convert to documents (to share to other members) or projects (if the change is presumed big)

Business Objects

Link Regulatory tracking processes and Intel to Business Objectives
Increase team productivity by having one platform for a more collaborative approach to regulatory compliance and risk management across the company (and subsidiaries)
Understand and properly communicate the regulatory risks
Effectively manage all these within right budget