FORMULATION AND PROTOTYPE
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AND PROFESSIONAL MANUFACTURING
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COSMETICS
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Labderma — laboratory journal13th of September, 202646.05°N · 14.51°E · Ljubljana, SI · Est. 2024
CPNP
— notification before sale in the EU
CPNP notification for cosmetic products
Notification of a cosmetic product through the European Commission's CPNP before the product is placed on the European Union market.
Notification
CPNP is a notification, not a marketing authorisation
CPNP does not pre-approve a cosmetic product. Notification is one part of the regulatory process. Before the product is placed on the market, the responsible person, CPSR, PIF, labelling and other required information must already be properly addressed.
Preparation
What must be ready first
The final formulation, responsible person, product and packaging details and supporting documentation must be sufficiently complete before the notification is finalised. If the PIF or CPSR is not ready, the documentation should be resolved first.
Responsibility
Responsible Person
Every cosmetic product placed on the EU market must have a designated Responsible Person established in the European Union. That entity carries the legal responsibility for product compliance. A laboratory may prepare documentation and support the notification process, but that does not automatically transfer the legal role of Responsible Person.
Questions
What clients ask most
Does CPNP issue an approval?
No. It is a mandatory notification system, not a pre-market authorisation.
Can you help with a product made outside the EU?
Yes, provided the required technical documentation is available or can be completed.
Next step
Write to us
Check what is missing before notification
Send us the product details, country of manufacture, Responsible Person information and the documentation you already have. We will identify what needs to be completed before CPNP notification. Related: PIF and CPSR · Stability testing · Challenge test