Compliance intelligence for regulated industries.
An independent external review layer that finds what internal teams miss, before regulators do. One methodology. Every regulated industry.
One platform. Eight regulated industries.
Choose your industry
What is Avidara
Not a consultancy. A compliance intelligence layer.
Avidara encodes the regulatory rulebook for your industry and applies it consistently, exhaustively, and independently — every review. The methodology is universal. Only the ruleset changes per vertical.
The market invested in compliance infrastructure. Avidara addresses compliance intelligence. That is the gap.
The findings are ours. The decisions are yours.
Speed beyond human capacity
Every PI reference cross-checked, every claim validated, every mandatory element verified — in parallel, not sequentially.
Exhaustive consistency
No reviewer fatigue. No commercial pressure. The same rigour from finding one to finding fifty — every single time.
Independence preserved
Avidara flags, analyses, and reports. Your team reviews, validates, and owns every decision. Control stays with you — always.
How it works
Three steps. Zero ambiguity.
You bring the document. Avidara brings the rulebook. You get a clear, structured finding report before anything leaves your desk.
New Review
Drop your document here
PDF, DOCX, XLSX, PPTX, JPG, PNG — max 50 MB
Cardivex_LeaveBehind_v2.pdf
2.8 MB · Reference PI: EVD-NX-001/SA · Ready
Finding Severity
Every finding is graded. Nothing is ambiguous.
Must be corrected before submission or release. Regulatory non-compliance that cannot proceed as-is.
Significant issue likely to cause a regulatory query, delay, or rejection. Should be resolved before submission.
Smaller inconsistency. Good practice to address before finalising.
A clean report is a good outcome, not an error. No findings means no significant discrepancies were detected — the report supports your compliance decision. It does not replace professional regulatory sign-off.
You receive a structured PDF report. Immediately.
Available for download the moment the review completes — no waiting, no follow-up required.
Why Avidara
Built differently, by design.
No internal bias
Avidara answers only to the regulatory rulebook, not to commercial timelines, marketing budgets, or launch pressure.
Intelligence, not checklists
Findings come with context — the exact PI section, why it matters, and what correction is required. Not a flag, a path forward.
Control stays with your team
Avidara produces findings. Your team reviews, validates, and owns every decision. We are a prerequisite to your compliance decision, never a substitute.
Universal methodology, vertical rulesets
The same analytical framework whether the document is a pharma PI, a transport permit, or a chemical SDS. Only the encoded ruleset changes.
Consistent at scale
No reviewer fatigue, no variation between team members. The same rigour from review one to review one thousand.
Structured for your MLR file
Every report formatted for direct inclusion in your Medical, Legal and Regulatory record — with version control, outcome status, and sign-off blocks.
Zero Data Retention — by design
All AI processing runs within Avidara's private cloud infrastructure. Your documents are never transmitted outside that environment, never stored after processing, and never used to train any model — by contractual terms and by architecture.
Always current.
Avidara monitors regulatory updates from SAHPRA, EMA, FDA, MHRA, TGA, Health Canada, PMDA, NAFDAC, and others — so the review framework reflects current requirements, not last year's guidelines.
Enterprise — now available
Built for teams. Embed it in your stack.
API access, single sign-on, audit trails, and concurrent review capacity — live today. Scale from a single reviewer to an enterprise compliance team without changing how it works.
REST API
Headless integration via avd_live_ keys, with HMAC-signed webhooks. Embed reviews directly into your DMS or workflow.
SSO / SAML 2.0
Single sign-on through Azure AD, Okta, and other corporate identity providers. No separate Avidara login.
Audit log
Full timestamped activity trail — demonstrate complete review history to auditors and regulators.
Usage analytics
Per-tenant dashboard: review volumes, service breakdown, and outcomes by document type.
Concurrency tiers
Multiple team members running simultaneous reviews — capacity scales with your plan.
Team workspaces
Separate, isolated environments per organisation or business unit.
Book a review
Ready to close your compliance gaps?
Two ways to engage — pick the one that fits your situation, or tell us what you need and we will recommend the right approach.
No commitment required. We will confirm scope and turnaround before any work begins.