The safe, smart search tool for biomedical and pharmaceutical guidance

Stop spending hours on something you can do in seconds! RegFast provides instant search for domestic and global pharmaceutical regulations and guidance.

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Comparison

Why Not ChatGPT?

While ChatGPT is a powerful tool, it lacks access to current regulatory documents. This fundamental limitation leads to outdated, incomplete, and sometimes incorrect information—especially in the complex world of pharmaceutical regulations. RegFast is purpose-built for pharma regulatory compliance, with direct access to authoritative source documents, ensuring you get reliable, current, and verifiable information every time.

Feature RegFast ChatGPT
Comprehensive answers
Thorough citations
Access to all source documents
No saved chats
No privacy liabilities
Features

Accelerate your research

Search regulations in natural language. Get instant answers, verify sources, and stay updated with the latest changes.

Lightning Fast Research

Get regulatory answers in seconds instead of hours.

Comprehensive Knowledge

Access worldwide regulations with direct links to sources.

Always Up to Date

Stay ahead with real-time updates to regulatory changes.

Worldwide Coverage

Access Global Regulations

Stay compliant across borders with comprehensive access to regulatory information from major health authorities worldwide. Our platform keeps you updated with the latest requirements and guidelines.

FDA

United States

EMA

European Union

PMDA

Japan

MFDS

South Korea

TGA

Australia

ICH

International

MHRA

United Kingdom

ANVISA

Brazil

NMPA

China

More

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Workflow Revolution

Stand Out

Give your team the competitive edge. While other teams are still searching through documents, your team will be moving projects forward with instant, authoritative insights. Break through gridlock, accelerate approvals, and prevent costly compliance errors before submission—becoming the regulatory experts that leadership trusts to get it right the first time.

Traditional Process

Search through multiple regulatory databases
Manually cross-reference documents
Wait for translations of foreign regulations

With RegFast

Instant answers from all regulatory sources
Real-time translation and cross-referencing
AI-powered reports with direct citations to source documents
Multilingual Support

Break language barriers

Our AI-powered system can read and understand regulations in any major language, providing you answers in your preferred language. No more language barriers in regulatory compliance. Languages include but are not limited to:

English
Japanese
Korean
German
Spanish
Portuguese
Mandarin
Arabic
Russian
Hebrew

What are the labeling requirements for medical devices in Japan?

医療機器の表示には、製造業者名、製品名、承認番号、使用期限などの情報を日本語で明確に表示する必要があります。

Medical device labels must clearly display information in Japanese, including manufacturer name, product name, approval number, and expiration date.

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