Register your cosmetic products and facilities with confidence. We help brands meet FDA and MoCRA requirements quickly and accurately — with expert guidance built for results.














We offer more than just product registration. Our consulting services cover every requirement for entering the U.S. market — from MoCRA compliance to FDA cosmetic facility registration. Each service is available individually or as part of a full FDA cosmetic product registration strategy.
We offer more than just product registration. Our consulting services cover every requirement for entering the U.S. market — from FDA compliance to MoCRA Facility Registration service. Each service is available individually or as part of a full FDA cosmetic product registration strategy.
We’ve helped startups and global cosmetic companies navigate complex FDA requirements — from initial registration to full MoCRA compliance. Our consulting is built for regulatory clarity, consistent results, and smooth market access.
Structured CPNP Data Pack (Article 13): A validated dataset with product category/name, RP details, country of origin, ingredient info, frame formulation, nanomaterial flags, CMR identifiers, and ready-to-upload label and product image.
Complete CPNP Filing & ID Confirmation: Creation or update of the notification for each SKU or variant, with CPNP IDs recorded for your PIF and regulatory logs.
Nanomaterials Timeline & Submission Handling: If applicable, planning and execution of Article 16 pre-notification — including six-month timelines and exceptions for listed colorants, preservatives, and UV filters.
We’ve helped startups and global cosmetic companies navigate complex FDA requirements — from initial registration to full MoCRA compliance. Our consulting is built for regulatory clarity, consistent results, and smooth market access.
Let’s simplify your U.S. market entry. Our consultants help you complete your cosmetic FDA registration, meet MoCRA compliance, and avoid costly regulatory delays. Whether you need one service or full support, we’re ready to guide you.
Yes. Under the new MoCRA law, all marketed cosmetic products in the U.S. must be registered with the FDA. This includes disclosing ingredients and responsible party information through the new FDA portal.
MoCRA (Modernization of Cosmetics Regulation Act of 2022) is a major update to U.S. cosmetic laws. It requires mandatory cosmetic product registration, facility registration, safety substantiation, and adverse event reporting. Compliance is now required for both U.S. and foreign brands.
No. The FDA does not “approve” cosmetics before they go to market. However, brands must complete FDA registration for cosmetics, ensure accurate labeling, and meet all safety requirements under MoCRA.
The initial deadline set by the FDA was July 1, 2024, for both domestic and foreign cosmetic facilities. Ongoing updates and annual renewals are required to remain compliant.
Yes. Foreign cosmetic companies must designate a U.S. Agent to represent them before the FDA. This is a MoCRA requirement and is essential for successful cosmetic FDA registration.
Absolutely. All of our services — including cosmetic facility registration, MoCRA compliance consulting, and U.S. Agent services — are available separately or as part of a complete support package.
Timelines vary depending on your product complexity and documentation. However, with complete information, we typically finalize FDA cosmetic product registration and facility submissions within a few business days.
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