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Compliance · US, UK, EU

Made in Korea,
cleared to sell where you sell.

Formula, labels and filings planned from the first sample, so your product can actually go on sale. We handle US MoCRA directly and run UK and EU launches through specialist partners, with every document from your Korean manufacturer collected up front.

Free and no commitment. We reply within 3 business days.

10+Brands launched
100+Korean SME manufacturers
$5KFirst orders from
14 to 18 wksConcept to shipment

Where are you selling?

Each market has its own rules, owner and timeline. Tell us your markets in your request and we plan for them from day one.

United States

MoCRA and FDA

$300 to $800 US compliance add-on
  • FDA facility and product registration
  • MoCRA product listing, within 120 days of launch
  • US Responsible Person, quoted separately
  • Label compliance and ingredient review
United Kingdom

UK Cosmetics Regulation

$2,200 to $3,700 per product, via partner
  • UK Responsible Person
  • Product Information File and safety assessment
  • SCPN notification before sale
  • UK labeling with your RP's details
European Union

Regulation (EC) 1223/2009

$2,200 to $3,700 per product, via partner
  • EU Responsible Person
  • PIF with CPSR, signed by a safety assessor
  • CPNP notification before sale
  • Labels in the language of each country

UK and EU costs cover the Responsible Person, safety assessment and notification for one market, converted from 3 to 5 million KRW. Stability, challenge and claim testing, translation, packaging changes and annual RP renewal are extra.

Compliance built in, not bolted on

Most launch delays start at the formula or the label. We catch them before you pay for production.

Ingredients checked for your markets

A formula that is legal in Korea can need changes for Europe. The EU now caps retinol at 0.3% retinol equivalent in face products, and fragrance allergen labeling expanded to about 80 allergens for new products from July 2026. We develop with your markets' rules from the first sample.

Labels designed to pass

Required English copy, INCI list, Responsible Person details and warnings, laid out to spec. Korean typography can sit alongside it for authenticity.

Manufacturer documents up front

CGMP / ISO 22716 certificates, INCI lists, MSDS / SDS and test reports. We ask for what your market needs before production, not when registration stalls.

Registered factories first

We primarily match you with manufacturers already FDA facility-registered. If the best factory isn't, we handle registration before production, with the cost usually shared with the manufacturer.

UK and EU timelines

SituationTypical timeline
All documents ready (ingredient data, CPSR, PIF complete)About 2 weeks to 1 month
Standard project from scratchAbout 2 to 6 months
Ingredient rework needed6 months to a year or more

Our advice: formulate with ingredients that comply in both the UK and the EU, launch in one, and expand later. The second market is then mainly paperwork.

From the field · US

A US brand was told it was small-business exempt and skipped registration. Weeks later a sales channel demanded MoCRA listing documents before approving the products. Listing was still inside the 120-day window, so we registered the products fast and got them cleared before the launch slipped.

From the field · UK

A London founder planning five products asked us, before paying anything, for a full roadmap and itemized budget: Responsible Person and notification, testing, packaging, freight, duties and VAT, and annual compliance. Seeing the whole bill first is exactly right for the UK.

Not sure what your market needs?

Tell us your product and where you'll sell. Your free estimate includes a market check, so compliance costs show up before you commit.

Start your request

Free price range within 3 business days. You only pay when you decide to start sampling.
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Frequently asked questions

Do I need to register my cosmetics with the FDA?

Under MoCRA, cosmetics sold in the US must be listed with the FDA, and listing is due within 120 days of going to market. Small businesses under $1M in average annual US cosmetic sales may be exempt from facility registration and product listing, but marketplaces such as Amazon increasingly ask for MoCRA proof anyway, and adverse-event reporting, safety substantiation and labeling still apply.

Does the FDA charge a fee?

No. The FDA does not charge for MoCRA registration or listing. You pay for the filing work, which through our network typically runs around $150 per product. A US Responsible Person, if you need one, is quoted separately.

Do I need separate registrations for the UK and the EU?

Yes. Great Britain uses SCPN with a UK-based Responsible Person, and the EU uses CPNP with an EU-based Responsible Person. Northern Ireland follows EU rules. Selling in both means two Responsible Persons and two notifications.

How much does UK or EU compliance cost?

Through an agency, the Responsible Person, safety assessment (CPSR) and notification typically run about $2,200 to $3,700 per product for one market, before testing, translation and packaging changes.

How long does UK or EU compliance take?

About 2 weeks to a month if every document is ready, 2 to 6 months from scratch, and longer if ingredients need rework. Planning the formula for your market from the first sample avoids most of the delay.

Keep reading

This page is general information, not legal advice. Rules and thresholds change; we confirm the current position for your products and markets during your project.