About RelyAInt
Built by compliance experts.
Powered by AI.
RelyAInt was built because regulated organisations deserve a faster, more structured way to identify compliance risk — without waiting weeks for an external consultant to tell them what their own team already suspects. We built the platform we wished existed.
1,400+
Regulatory controls in our GxP library
48hrs
From evidence upload to full assessment with remediation actions
12+
Global regulatory frameworks covered
FDA · EMA · MHRA · SAHPRA
AI-assisted. Human-governed.
Platform — not advisory
Our story
Why RelyAInt exists
The compliance problem in regulated pharma isn't a lack of knowledge — it's a lack of structured, accessible tooling that puts that knowledge in the hands of the people who need it most.
The problem
Traditional compliance is slow, expensive, and opaque
Regulatory consultants charge $200–$400/hour. A single GAP assessment takes 4–8 weeks. Findings arrive in a PDF that your team must manually translate into actions. And when the inspector arrives, the paper trail depends entirely on how well the consultant documented their thinking — not yours.
The insight
Your team already knows most of what needs fixing
Experienced QA professionals and validation leads understand their systems. What they lack is a structured framework to surface, classify, and act on compliance gaps — and a workflow that produces inspection-defensible documentation without starting from a blank page every time.
The platform
AI-accelerated. Human-governed. Inspection-ready.
RelyAInt gives your team's qualified employees a structured compliance workflow — AI classifies severity and surfaces findings, your team confirms and manages actions, and every determination is traceable. Expert review is available on demand when you need it.
The result
48 hours instead of 8 weeks
Upload your evidence, run your assessment, review AI-classified findings, manage corrective actions, and generate an inspection-ready report — all within 48 hours of your team starting work. No waiting for a consultant. No blank pages. No opaque methodology.
What drives us
Platform values that mean something
Not generic values lifted from a professional services brochure. Values that directly govern how the platform is built, governed, and delivered.
Regulatory primacy
Every control, finding, and recommendation is anchored in the primary regulatory requirement — not best practice, not convention, not what auditors usually want.
Human accountability
AI accelerates and classifies — your qualified team confirms. No compliance determination leaves the platform without human sign-off. This is non-negotiable and built into the workflow.
Inspector explainability
Every output is designed to be explained to an inspector. If the logic cannot be traced from evidence to finding to action, it does not belong in the platform.
Risk proportionality
Effort is allocated by risk — not by convention or completeness. Critical findings get immediate attention. Minor findings get documented rationale. Everything is proportionate.
Radical transparency
The platform shows its working. Every AI classification is visible, every human confirmation is logged, and every evidence link is traceable. No black boxes in regulated compliance.
Global reach
FDA · EMA · MHRA · SAHPRA · TGA · WHO · ICH — built for the reality that regulated organisations operate across multiple jurisdictions simultaneously.
Platform differentiators
What makes RelyAInt different
Four capabilities that separate a compliance platform from a compliance document.
Inspector-explainable outputs
Every finding, action, and report is structured for regulator explainability. Your team can hand any output to an inspector and trace the complete decision logic from evidence to conclusion.
Platform-enforced governance
Governance is built into every workflow step — not bolted on. Human confirmation of regulatory applicability and GAP conclusions is required before any finding is published. The platform enforces this, not the individual.
Risk-prioritised findings
AI classifies every finding as Critical, Major, or Minor based on regulatory impact and business urgency. Your team confirms the classification. Corrective actions are automatically generated and assigned in the portal.
Self-serve with expert escalation
Your qualified employees run assessments, review findings, manage actions, and upload evidence entirely within the platform. When your team needs additional assurance, a RelyAInt expert is available on demand — not as the default.
AI governance
How AI and humans work together in the platform
RelyAInt uses AI to accelerate what machines do well — pattern detection, cross-referencing, severity classification, and drafting. Everything that requires regulatory judgement is confirmed by a qualified human. This is not a policy statement — it is how the workflow is built.
AI accelerates the full assessment workflow
Reviews documents, flags anomalies, assigns severity classifications, and drafts corrective actions — your team confirms each one
Your team governs every determination
All AI-assigned classifications are reviewed and confirmed by your qualified employees before any finding is published
Expert escalation available on demand
When your team needs additional assurance, a RelyAInt expert can review any finding or report — requested directly from the platform
Regulatory coverage
Built for global compliance
Our regulatory library covers 1,400+ controls across every major GxP framework — mapped, cross-referenced, and kept current across jurisdictions.
North America
FDA 21 CFR
FDA Guidance
Health Canada
Europe
EMA Annex 11
EU GMP
MHRA
Africa & Asia-Pacific
SAHPRA
TGA
NAFDAC
ZAZIBONA
International
WHO GMP
ICH Q-Series
PIC/S
GAMP 5
1,400+
GxP regulatory controls in the library
12+
Global regulatory frameworks covered
4+
Regions — FDA, EMA, Africa, Asia-Pacific
See it for yourself
Try the platform — no sign-up needed.
Run a preliminary compliance assessment on our homepage. Describe your situation, get AI-assisted findings in seconds, and see how the platform structures compliance work for your team.
No obligation
No sign-up required
Results in seconds
Human-governed follow-up available