ZentraReg AI — Regulatory Intelligence, Engineered by AI
The ultimate AI-powered Chat Advisor dedicated to ICH, FDA, and EMA guidelines. Navigate
complex pharmaceutical regulations and validate your documents with unprecedented speed and precision.
Expert Chat Advisor
Instantly resolve regulatory ambiguities by chatting with an AI trained directly on official agency guidelines
and directives. Get accurate interpretations of Quality, Safety, Efficacy, and Multidisciplinary guidelines.
Document Validation
Upload proprietary PDFs and Word documents securely. Rapidly validate structures, claims, and formats against
current ICH, FDA, and EMA regulations.
Why ZentraReg AI?
- Instant Answers — Get precise regulatory guidance in seconds, not hours of document searching.
- 700+ Official Guidelines — Trained on ICH Quality (Q), Safety (S), Efficacy (E), and Multidisciplinary (M) guidelines.
- Enterprise-Grade Privacy — Zero-retention AI processing. Your data is never used to train models.
- Document Analysis — Upload SOPs, protocols, and submissions for instant compliance validation.
Built on Trusted Regulatory Sources
ZentraReg AI draws from a comprehensive database of official pharmaceutical regulatory documents, ensuring every answer
is grounded in authoritative guidance from the world's leading regulatory bodies:
- ICH — International Council for Harmonisation
- FDA — U.S. Food and Drug Administration
- EMA — European Medicines Agency
Key Features
- ICH guideline expert chat with source citations
- FDA regulatory compliance verification
- EMA guideline interpretation
- Secure document upload and AI-powered validation
- Covers Quality, Safety, Efficacy, and Multidisciplinary guidelines
- Free tier: 5 questions/day, 50 questions/month
Frequently Asked Questions
What is ZentraReg AI?
ZentraReg AI is an AI-powered regulatory intelligence platform that helps pharmaceutical professionals navigate ICH, FDA,
and EMA guidelines. It provides instant, source-cited answers to complex regulatory questions and can validate uploaded
documents against current compliance requirements.
Which guidelines does ZentraReg AI cover?
ZentraReg AI covers over 700 official regulatory documents including ICH Quality guidelines (Q1–Q14), Safety guidelines
(S1–S11), Efficacy guidelines (E1–E20), and Multidisciplinary guidelines (M1–M13), as well as selected FDA and EMA guidance documents.
Is my data safe with ZentraReg AI?
Yes. ZentraReg AI uses enterprise-grade Google Cloud infrastructure with zero-retention AI processing. Your queries and
uploaded documents are never used to train or improve AI models. All data is encrypted in transit (TLS 1.3) and at rest (AES-256).
Can I use ZentraReg AI for free?
Yes. ZentraReg AI offers a free tier with 5 questions per day and 50 questions per month. Premium subscribers get unlimited
access, enhanced document upload capabilities, and priority processing.
Can I upload my own documents for AI analysis?
Yes. You can securely upload PDF, DOCX, and PPTX files for AI-powered compliance analysis. Uploaded documents are processed
transiently and are never stored beyond the active analysis session.
Powered by Aezis AI
ZentraReg AI is built by Aezis AI, providing cutting-edge regulatory
intelligence for pharmaceutical professionals, regulatory affairs specialists, and quality assurance teams.
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