Global cosmetic regulatory compliance

One regulatory partner.Five market routes.

Local Responsible Person entities in the EU, UK and Türkiye, with coordinated notification and market-entry support for the USA and Canada.

EU · UK · TR3 local entitiesUSA · CA5 priority marketsB2BStructured proposal
01

BudapestEU Responsible Person entity

02

LondonUK Responsible Person entity

03

IstanbulTürkiye regulatory entity

QMS

ISO 9001Quality-management documentation

Free pre-assessment

Is your cosmetic product market-ready?

Select a target market and record the evidence already available. The result highlights the next operational priorities.

01Complete quantitative formula and final INCI list
02Final or draft market-specific label artwork
03Safety evidence, raw-material specifications and certificates
04Stability, compatibility, microbiology and challenge-test position
05Responsible Person or local responsible route confirmed
06Product notification or listing route confirmed

End-to-end regulatory scope

From formula review to market continuity.

Safety assessment, documentation, notification and representation are coordinated through one accountable operating model.

01EU RP

EU Responsible Person

Local EU representation, compliance oversight and authority coordination under Regulation (EC) No 1223/2009.

Learn more
02UK RP

UK Responsible Person

A Great Britain market route combining local representation, SCPN readiness and compliant label particulars.

Learn more
03CPSR

CPSR & Product Information File

Scientific safety assessment and a structured PIF prepared for market access, inspection and lifecycle updates.

Learn more
04CPNP

Product Notifications

Coordinated submission support for CPNP, SCPN, ÜTS and other market-specific cosmetic notification workflows.

Learn more
05ART 19

Label & Claims Review

Market-specific artwork screening for mandatory particulars, language, warnings, claims and ingredient presentation.

Learn more
06ISO

Cosmetic Testing Coordination

Laboratory planning and evidence review for microbiology, challenge, stability, compatibility and claim support.

Learn more

Market-specific execution

Local accountability where it is required.

We clearly distinguish local Responsible Person entities from regulatory support markets, so your route to compliance is transparent from day one.

EU
BudapestLocal Kompass Europe entity

European Union

EU Responsible Person and full Regulation (EC) No 1223/2009 market-access support through our Hungarian entity.

  • Responsible Person
  • CPSR, PIF and CPNP
  • EU label and lifecycle compliance
Learn more
UK
LondonLocal Kompass Europe entity

United Kingdom

Local UK Responsible Person, SCPN submission and Great Britain label review through our London entity.

  • UK Responsible Person
  • SCPN notification
  • GB-specific label assessment
Learn more
TR
IstanbulLocal Kompass Europe entity

Türkiye

Local company support for ÜTS, responsible technical personnel, Turkish PIF and label compliance.

  • ÜTS workflows
  • Responsible technical personnel
  • Turkish documentation and label
Learn more
USA
MoCRARegulatory support market

United States

FDA MoCRA facility registration and product listing support for foreign cosmetic businesses.

  • Facility registration
  • Product listing
  • Safety and record readiness
Learn more
CA
Health CanadaRegulatory support market

Canada

Health Canada CNF, Cosmetic Ingredient Hotlist and bilingual label support; not a local Kompass Europe entity.

  • CNF preparation
  • Hotlist review
  • English-French label requirements
Learn more

Controlled delivery

A clear route from evidence to launch.

Each engagement is scoped by product, market and regulatory risk. You always know what is required, what is missing and what happens next.

Discuss your project
  1. 01

    Define markets

    Confirm product scope, launch countries and commercial priorities.

  2. 02

    Review evidence

    Screen formula, raw-material, testing, packaging and claims documentation.

  3. 03

    Build compliance

    Prepare the required safety files, labels and notifications.

  4. 04

    Maintain control

    Manage updates, authority requests and lifecycle changes.

Regulatory intelligence

Current developments, translated into action.

Official updates from EU, UK, USA and Canada, interpreted for cosmetic manufacturers and brand owners.

UK

OPSS publishes new SCPN safety data

UK authorities report 861,686 SCPN notifications and continued action on prohibited ingredients.

Learn more
CA

Canada expands fragrance-allergen labelling

For new cosmetics, the Canadian disclosure list expands to 81 fragrance allergens from 1 August 2026.

Learn more
USA

FDA updates Cosmetics Direct for biennial renewals

FDA added renewal status, reminders and updated instructions for MoCRA facility registrations.

Learn more

Due-diligence ready

Corporate evidence, not marketing claims.

Company information, quality credentials, assessor competence and verification channels are brought together in one transparent Trust Centre.

Trust Centre
01

Corporate identity

Hungary, United Kingdom and Türkiye entity information.

02

Professional competence

Safety-assessor qualification and recognition evidence.

03

Verification channel

Product representation, complaints and unauthorized-use reporting.

Structured project enquiry

Request a regulatory proposal

Tell us the essentials. We will return the appropriate scope, required evidence and next steps.

Target markets *

Your enquiry is routed to the regulatory team and receives a reference number.