EU
EU market placement (CPNP + PIF)
Notify via CPNP and structure the Product Information File so products can be placed on the EU market.
Best for: Brands entering or expanding in the EU/EEA.
Talk to usServices
Services
From decision to market access — diagnostics and partner-fulfilled execution.
- EU, US & China
- Project-based work
- Quote after diagnostic
How it works
-
1
Diagnose
Markets, product type, timeline, and constraints.
-
2
Scope & quote
Written track, roles, and commercial proposal.
-
3
Execute
Specialists deliver registration, RP, safety files, or tests under clear ownership.
-
4
Track
Status visibility with CosmeticsBridge as your single relationship.
Service catalog
Filter by market. Packages are quoted after diagnostic — not a price list for regulated work.
Market access
EU
EU Responsible Person
Establish an EU-based Responsible Person pathway with clear roles, labeling impact, and ongoing duties.
Best for: Non-EU brands that need an RP of record.
Talk to us
EUUK
CPSR — cosmetic product safety report
Coordinate a toxicologist-signed safety assessment aligned with EU/UK expectations.
Best for: Any brand needing a compliant safety file before placement.
Talk to us
UK
UK market placement (SCPN + PIF)
UK notification and PIF readiness for Great Britain market access.
Best for: Brands selling into the UK post-Brexit pathways.
Talk to us
US
US MoCRA facility listing
Map and complete facility listing obligations under MoCRA.
Best for: US and foreign manufacturers / processors serving the US market.
Talk to us
US
US MoCRA product listing
List products with FDA on the required cadence and keep listings current.
Best for: Brands with cosmetics in US commerce under MoCRA.
Talk to us
US
US cosmetics labeling readiness
Review labels and claims against US expectations before launch or rework.
Best for: SME brands preparing packaging for the US.
Talk to us
China
China general cosmetics notification
Prepare and drive general cosmetics notification with dossier discipline.
Best for: Overseas brands entering China with general cosmetics.
Talk to us
China
China special cosmetics registration
Scope special categories (e.g. sunscreen, hair dye, whitening) and manage registration milestones.
Best for: Brands with products classified as special cosmetics in China.
Talk to us
China
China domestic responsible person
Appoint and run a China domestic responsible person for filings, communication with authorities, and post-market duties.
Best for: Overseas brands that need a China domestic responsible person of record.
Talk to us
China
China import & export compliance
Support import/export pathways for cosmetics into or out of China — classification, paperwork orientation, and coordination with local specialists.
Best for: Brands and traders shipping cosmetics across the China border.
Talk to us
China
China safety assessment dossier
Coordinate safety assessment documentation to Chinese technical expectations.
Best for: Brands preparing notification or registration packages.
Talk to us
China
China cosmetic ingredient notification
Ingredient submission / notification support, including submission codes and supplier data packages for China filings.
Best for: Ingredient suppliers and brands that must file raw-material data in China.
Talk to us
China
New cosmetic ingredient (NCI)
Support new ingredient registration or notification, monitoring, and data-gap planning.
Best for: Ingredient suppliers and brands introducing NCIs in China.
Talk to usProduct integrity
EUUSChinaUKMulti
Formula & ingredient compliance review
Screen formulas against target-market restrictions before costly reformulation.
Best for: R&D and RA teams launching or reformulating SKUs.
Talk to us
EUUSChinaUKMulti
Label & claims review
Align pack copy and claims with market rules and reduce over-claim risk.
Best for: Marketing + RA co-review before print or digital launch.
Talk to usAdvisory
EUUSChinaUKMulti
Project diagnostic
Clarify markets, product type, timeline, and the right service track — before you commit budget.
Best for: Any brand unsure what “done” looks like for a market entry.
Talk to us
EUUSChinaUKMulti
Fractional regulatory support
Ongoing RA bandwidth for SMEs that cannot staff a full compliance team.
Best for: Founders and one-person regulatory roles.
Talk to usASEAN, Japan, Korea, Middle East and other markets are available on request through our specialist network.
Starter packages
EU Starter
Path diagnostic for CPNP / RP / CPSR: what you need first, what can wait, and a clear project outline.
US MoCRA Starter
Facility and product listing readiness with an SME checklist and submission plan.
China Entry
General notification readiness: classification, dossier gaps, RP options, and testing orientation.
Quoted after diagnostic. Fixed packages available where scope is standard.
Specialist network
Execution is delivered through vetted specialists — including EU/UK cosmetics consultants (for example Taobe Consulting pathways) and China/global compliance specialists. CosmeticsBridge remains your single commercial relationship and project owner.
We are not a testing laboratory and do not replace official authorities. Reports and RP appointments are issued by the appropriate licensed or appointed parties in each jurisdiction.
From intelligence to a project
Already following updates on CosmeticsBridge? Turn a News item, Insight, or Workbench case into a scoped execution project.
Request a project diagnostic
Tell us markets, product type, and timing. We reply with a recommended track — free diagnostic for serious enquiries.
FAQ
Are you a testing lab or the EU Responsible Person of record?
No. We coordinate and manage the project. Labs, RP entities, and signing toxicologists are specialist parties in the delivery network.
How is this different from membership?
Membership is ongoing regulatory intelligence and Workbench tools. Services are project-based market access and compliance execution.
Do you cover ASEAN, Japan, or Middle East?
Yes on request via our network. Lead with EU, US, or China for the fastest path; other markets are scoped after diagnostic.
Is this legal advice?
No. Services support regulatory compliance work products. Formal legal opinions require qualified counsel where needed.