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N

Noedal

S. Modernization of Cosmetics Regulation Act (MoCRA) and other regulated markets.

Updated 2 months ago

Funding

Funding not disclosed

Funding rounds are not available yet.

Founders

Founder details are not available yet.

Product

Problem

Cosmetics companies must navigate complex, time‑consuming regulatory filings for the U.S. Modernization of Cosmetics Regulation Act (MoCRA) and other markets, often relying on manual processes, costly consultants, and fragmented communication with manufacturers.

Solution

Noedal offers a cloud‑based platform that automates MoCRA compliance by connecting directly to the FDA’s database and providing drag‑and‑drop ingredient workflows. The system generates FDA 5067 product listings and 5066 facility registrations, validates ingredient INCI and UNII data, and supports auto‑renewal. Integrated collaboration tools let brands and manufacturers exchange documents within a secure vault, while AI‑assisted label review and human expert checks ensure filing accuracy. Centralized records also enable easy expansion into additional regulated markets such as the EU CPNP, China NMPA, and Southeast Asian authorities.

Target Audience

Primary users are cosmetics brands and product manufacturers that need to file MoCRA submissions and plan to enter other regulated markets, as well as regulatory consultants managing multiple client filings.

Features

  • Direct, real‑time connection to the FDA database for automated filing of product listings (Form 5067) and facility registrations (Form 5066)
  • Drag‑and‑drop ingredient file upload with automatic INCI/UNII validation and FDA form generation
  • Secure Document Vault for ingredient files, certificates, and regulatory forms, shared between brands and manufacturers
  • Manufacturer Collaboration module that allows suppliers to upload data directly, eliminating email back‑and‑forth
  • AI‑assisted Label Reviewer that checks ingredient lists and formatting against FDA requirements, with human expert oversight
  • Auto‑renewal and real‑time status tracking for ongoing compliance and annual updates
  • Multi‑market scalability framework to extend compliance workflows to EU CPNP, China NMPA, and SE Asia regulations
This profile is AI-generated and may contain inaccuracies.