Claims that hold up. Labelling that complies.
From health claims on supplement packaging to cosmetic ingredient disclosures, Avidara reviews every product communication against the applicable regulatory requirements — before your product hits shelves.
Minutes.
Report in your inbox, fast
50+
Regulatory frameworks encoded
100%
Your control preserved
Zero gaps
Consistent every review
Active Reviews
AVD-00042
Review in progress · In Review
AVD-00039
Previous review · Complete
AVD-00031
Queued document · Pending
Compliance Review — AVD-00042
Consumer Health · Nutraceuticals · Cosmetics · Document analysis complete
Findings
Critical non-conformance identified. Requires correction before approval.
Major deviation from regulatory requirement. Action required.
Incomplete supporting documentation. Cross-reference missing.
Minor formatting non-conformance. Advisory.
The challenge
One unsubstantiated claim can halt a product.
Consumer health is a high-stakes regulatory environment. Health claims, ingredient declarations, labelling formats, and marketing copy are all subject to specific regulatory requirements. A claim that feels acceptable to marketing can be a critical non-conformance in a SAHPRA review.
Avidara applies the applicable regulatory ruleset — whether R146, SAHPRA cosmetics guidelines, or the Foodstuffs Act — before your product lands in trouble.
Unsubstantiated health claim
"Clinically proven to boost immunity" on supplement packaging. No clinical study cited, no regulatory authorisation for that claim. Recall risk if flagged post-launch.
Prohibited ingredient not declared
Active ingredient classified as a scheduled substance present in formulation but not reflected on the label. Triggers immediate regulatory action.
Misleading "natural" claim
Product marketed as "100% natural" contains a synthetic preservative. Claim is false under R146 regulations and the Consumer Protection Act.
Net content labelling error
Net content declared as grams without mandatory metric equivalents. Non-conformance with Regulation 146 labelling requirements.
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 industry.
"The market invested in compliance infrastructure. Avidara addresses compliance intelligence. That is the gap."
The findings are ours. The decisions are yours.
01
Speed beyond human capacity
Every PI reference cross-checked, every claim validated, every mandatory element verified — in parallel, not sequentially.
02
Exhaustive consistency
No reviewer fatigue. No commercial pressure. The same rigour from finding one to finding fifty — every single time.
03
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
ImmunoBoost_Label_Final_v3.pdf
0.9 MB · Reference: R146 Regulations · Ready
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.
Not in Consumer Health?
Avidara serves multiple regulated industries with the same analytical rigour — only the ruleset changes.
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.