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Global Regulatory Documents

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Health Authorities Monitored

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Cloud-Based Access

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Daily Update Monitoring

Platform Features

Vistaar Capabilities & Your Benefits

Comprehensive capabilities engineered for global biopharmaceutical compliance and
regulatory intelligence.

regulatory-requirements-pharma

Regulatory requirements for Drugs, Biologics, OTC, and Generics products

manually-reviewed

Manually reviewed regulatory summaries covering clinical, technical, QMS/Quality, market launches, testing standards, submission checklists, fees, labeling, import/export, marketing, safety/Vigilance, life cycle requirements, and many more areas in a granular manner

translated

Translated Guidance documents and timely alerts

global-pharmacovigilance

Over 2 Million Global regulatory document repository of health authorities’ regulations and guidance, updated daily and provided to you with AI-enabled search for faster and better match

impact-assessment-pharma

Impact assessment, tracking, compliance matrix, projects/tasks and reports to o manage full cycle activity from monitoring to alerts review to share/assign to members, perform global impact assessment and finalize next steps

document-repository

Full project management functionality included as standard functionality

secure cloud

Cloud based with intuitive easy-to-use tool

integrated-submission

Using our built-in interfaces, integrate with any of your existing EDMS/RIM/Quality systems for exchange data or documents, if needed

For more information about Biopharma Regulatory
Intelligence & Compliance software

Book a Demo

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Insights and Updates

Regulatory Intelligence Database for Global Compliance and Strategic Decision-Making

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Pharma – Asia, S America, MENA, ROW Regulatory News –  Oct 2025

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Pharma – Asia, S America, MENA, ROW Regulatory News – Sept 2025

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Got Questions?

FAQ's

Find answers to frequently asked questions about Vistaar's Biopharma platform.

What is Vistaar's Biopharma Regulatory Intelligence & Compliance software?
Vistaar is a cloud-based platform that combines global regulatory data with project management workflows. It helps pharmaceutical and biotechnology companies track regulations, review updates, assess global impact, and ensure compliance for drugs, biologics, OTC, and generic products across health authorities worldwide.
What types of products and regulatory areas does Vistaar cover?
Vistaar covers drugs, biologics, OTC (over-the-counter), and generic products. It provides manually reviewed summaries across areas such as clinical requirements, technical standards, QMS/quality, submission checklists, market launches, fees, labeling, import/export rules, safety/vigilance, and product lifecycle management.
How many regulatory documents are available in Vistaar's repository?
Vistaar features a repository of over 2 million global regulatory documents and health authority guidelines. The database is updated daily and uses AI-enabled search to deliver fast, accurate regulatory matches and translated guidance documents.
Can Vistaar integrate with existing EDMS, RIM, or Quality systems?
Yes. Vistaar includes built-in interfaces that allow seamless data and document exchange with existing Regulatory Information Management (RIM), Electronic Document Management Systems (EDMS), and Quality Management Systems (QMS).
The First Step

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