Process

How EU & UK Cosmetic Compliance Works

From formulation to market placement under regulatory control.

Step 0

Required Inputs

The following information is required to initiate the regulatory process.
Input Format
Full formulation (% w/w) Excel
INCI list Text
Raw materials (supplier + trade names) List
Certificates of Analysis (where available) PDF
Label artwork JPG / PDF
Initial Review
  • Assessment of formulation (INCI) and available documentation
  • Preliminary identification of compliance gaps

Compliance Gap Analysis
  • Detailed assessment against EU and UK cosmetics legislation
  • Identification of non-compliant elements

Documentation Preparation
  • Preparation of Cosmetic Product Safety Report (CPSR – Part A and Part B)
  • Compilation of Product Information File (PIF)
Notification Submission
  • Submission to Cosmetic Products Notification Portal (CPNP) for the EU
  • Submission to Submit Cosmetic Product Notification (SCPN) for the UK
Final Compliance Validation
  • Verification that all regulatory requirements are fulfilled
  • Confirmation of readiness for market placement

Process Flow

Data → Market → Monitoring

Data

CPSR

PIF

Notification

Market Placement

Monitoring

Six Regulatory Steps

Step-by-Step Process

1–2 days

Data Review

Verification of formulation, INCI list, raw material data and label artwork against EU and UK regulatory requirements.

5–10 days

CPSR Preparation

Preparation of the Cosmetic Product Safety Report, Part A (safety information) and Part B (safety assessment) by a qualified safety assessor.

2–3 days

PIF Compilation

Compilation of the Product Information File: product description, GMP statement, CPSR, proof of claimed effects and animal testing data.

1–2 days

Notification

Submission to CPNP (European Union) and / or SCPN (United Kingdom) prior to market placement.

Final check

Market Placement

Label verification and final compliance check before the product is legally placed on the EU or UK market.

Ongoing

Post-Market Compliance

Serious Undesirable Effects (SUE) handling, market surveillance response, recall support and PIF maintenance throughout the product lifecycle.

FAQ

Frequently Asked Questions

Can you act as the Responsible Person for non-EU/UK brands?
Yes. Manufacturers outside the EU or UK must appoint a Responsible Person established in the respective market.
A complete formulation, ingredient list (INCI), and label artwork are typically required to start.
Yes. Products must be notified separately in the EU (CPNP) and UK (SCPN).
Yes. We review labels to ensure they meet regulatory requirements before market placement.

Required Input from Client

Deliverables

Legal Basis

Indicative Timeline

Standard regulatory cycle from data review to notification:

7–15 days

Subject to completeness of inputs and product complexity.
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