Cosmetica
About Cosmetica

Cosmetic compliance,
rebuilt on AI.

Cosmetica is an AI-powered regulatory compliance platform for cosmetics and personal care brands. We replace the consultants, the spreadsheets, and the manual FDA portal clicking with automated, citation-backed software covering 15 global markets.

The problem we're solving

In December 2022, the United States passed the Modernization of Cosmetics Regulation Act (MoCRA) — the most significant update to U.S. cosmetics law in over 80 years. The European Union has had similar requirements under EC 1223/2009 for over a decade. The UK has SCPN. Canada has the Cosmetic Ingredient Hotlist. And eleven more jurisdictions each have their own rules, portals, and language requirements.

For most cosmetics brands, the response has been to hire a regulatory consultant ($150–450/hour), use a single-market submission service like Registrar Corp, or wing it. None of these scale. A typical indie brand with ten products spends $35,000–$50,000 per year on compliance work that is repetitive, error-prone, and slow.

What Cosmetica does differently

Cosmetica is built around three convictions:

  • Regulatory work is mostly pattern-matching. Checking an ingredient against the EU Annexes or FDA CFR is the kind of task large language models are exceptionally good at — when grounded in the right source documents.
  • Citations matter more than answers. A regulatory finding without a source is worthless. Every result we surface links directly to the underlying SCCS opinion, CIR review, FDA CFR section, EU Annex entry, or PubMed study. No hallucinations.
  • Submissions should be programmatic. The FDA's ESG NextGen API supports automated submission of SPL XML files. We use it. There's no reason a product listing should require manually clicking through a portal.

The result is software that does compliance at roughly 15–40× the cost-efficiency of hiring for an equivalent capability set.

Who's behind Cosmetica

Cosmetica is built by The Zena Group, an independent software studio based in the United States. Our team works at the intersection of regulatory compliance, AI engineering, and product design.

We chose cosmetics because it's a category we know well, the regulatory burden has been growing for decades, and the tooling has been stuck in the early 2000s. MoCRA was the inflection point — for the first time, every U.S. cosmetic brand has direct FDA obligations, and the software market for handling them was wide open.

How we operate

250+ verified sources

Our knowledge base draws from SCCS scientific opinions, CIR safety reviews, the full FDA CFR (21 CFR Parts 700–740), EU Cosmetics Regulation Annexes II–VI, and indexed PubMed studies.

15 markets, one platform

United States, European Union, United Kingdom, Canada, Japan, South Korea, China, Australia, Brazil, India, Singapore, Thailand, UAE, Mexico, Taiwan.

Direct FDA ESG submission

Full integration with the FDA's Electronic Submissions Gateway NextGen API for facility registrations and product listings via SPL XML.

Enterprise-grade security

Data encrypted at rest (AES-256) and in transit (TLS 1.3). Per-tenant isolation on AWS. Formulation data never leaves our infrastructure.

AI you can audit

We use Claude Sonnet 4.6 via AWS Bedrock as the analysis engine. Every output links to a verifiable source — no model-generated regulatory text.

Built for real workflows

MedWatch 3500A automation, EPR tracking across 7 U.S. states, PIF builder, bilingual label generation, biennial renewal tracking.

Get in touch

For demos, partnership inquiries, or regulatory questions, reach us at hello@getcosmetica.com. For press, contact press@getcosmetica.com.

See pricing