Ask questions naturally: "What are the FDA requirements for AI in clinical trials?" or
"How do I submit to EMA?" REXI understands context and provides instant, accurate answers.
When you need to know, Ask REXI.
Three Ways to Chat with REXI
REXI Insights: Ask
About Regulatory Changes
What REXI does:
Provides real-time regulatory intelligence
and insights. REXI tracks updates from major
agencies like the FDA, EMA, and WHO, so
you don't have to.
Why Ask REXI:
REXI helps you deploy new AI projects
with confidence and ensures your operations
align with the latest guidelines. Ask REXI to
reduce time spent on compliance
assessments so you can focus on innovation.
REXI Review: Ask About
Promotional Materials
What REXI does:
Automates review and approval of
promotional materials. REXI uses
advanced AI to check your content
against comprehensive compliance rules,
ensuring it's ready for any channel.
Why Ask REXI:
Your marketing and sales teams get
materials to market faster, with less
risk of non-compliance. REXI learns
from every approval, making your
process more efficient over time.
REXI Connect: Ask
About Your Data
What REXI does:
Integrates and fuses data from
multiple sources— such as CMS
FHIR, PubMed, and ClinicalTrials.gov—
into a single, unified view.
What REXI does:
REXI connects the dots between
scientific literature, clinical trial data,
and regulatory information,providing
complete answers for better decision
-making and stronger audit trails.
REXI Knows the Way
Accelerated Timelines
Visit AskREXI.com and get instant
answers. We've seen dramatic
reductions in time spent managing
regulatory changes and launching
new projects.
Reduced Costs
AskREXI.com automates
repetitive compliance tasks,
helping you save significant
resources in regulatory
operations.
Peace of Mind
With AskREXI.com's real-time
monitoring and clear audit trails,
deploy new technologies and
launch products with
confidence.
Why REXI Knows Best
19
Jurisdictions
600+
Regulations
10
Free Queries/Day
Who Uses AskRexi
Regulatory Affairs Teams
Stay ahead of regulatory changes. Get instant notifications
about updates that affect your submissions and ensure
compliance across all jurisdictions.
✓ Real-time regulatory change alerts
✓ Multi-jurisdictional requirement comparison
✓ Submission pathway guidance
Compliance Directors
Ensure zero missed requirements across global operations.
Get comprehensive visibility into regulatory obligations and
compliance status.
✓ Portfolio-wide compliance monitoring
✓ Automated compliance validation
✓ Risk-based compliance prioritization
Proven Results
Industry-Leading First-Time Approval Rate
Zero
Missed Requirements
Industry-Leading
Approval Rate
19
Jurisdictions