Data review
1–2 days
Review formulation, INCI list, raw material data, and label artwork.
Process
How EU & UK Cosmetic Compliance Works
A practical process from product data to compliant market placement documentation.
Required inputs
| Input | Format |
|---|---|
| Full formulation % w/w | Excel |
| INCI list | Text |
| Raw materials, suppliers, trade names | List / Excel |
| Certificates of Analysis where available | |
| Label artwork | PDF / JPG / AI |
| Product type and intended use | Text |
| Intended market | EU / UK / both |
| Packaging information | Text / PDF |
| GMP information | PDF / statement |
Step-by-step process
Compliance gap analysis
Identify non-compliant or missing elements.
CPSR preparation
5–10 days depending on complexity
Prepare CPSR Part A and Part B.
PIF compilation
2–3 days
Compile the Product Information File.
Notification
1–2 days
Submit through CPNP and/or SCPN.
Market placement validation
Final label and documentation check before placing the product on the market.
Post-market compliance
SUE handling, authority requests, recall support, PIF maintenance, and regulatory monitoring.
Typical regulatory cycle: 7–15 working days, subject to completeness of inputs and product complexity. This is indicative and not guaranteed.
Request assessment
Prepare your product data for review
Send the INCI or formulation, product type, intended market, label artwork where available, and raw-material information where available.