{"id":520,"date":"2019-07-11T07:53:57","date_gmt":"2019-07-11T07:53:57","guid":{"rendered":"http:\/\/www.proersa.com\/eng\/?p=520"},"modified":"2019-07-11T07:53:57","modified_gmt":"2019-07-11T07:53:57","slug":"cosmetic-regulation-aerosol","status":"publish","type":"post","link":"http:\/\/www.proersa.com\/eng\/cosmetic-regulation-aerosol\/","title":{"rendered":"All you need to know for the marketing authorisation of a cosmetic aerosol"},"content":{"rendered":"

All you need to know for the marketing authorisation of a cosmetic aerosol<\/h1>\n

In this article, we want to highlight a not so visible part of\u00a0 the development cycle of an aerosol. This week we are talking about the imperatives linked with the marketing of a new cosmetic product. How to be sure that you are complying with the rules ?<\/p>\n

Our framework of study will be contained among the European Union, with the European cosmetic regulation 1223\/2009. This regulation has multiple goals. It makes sure that any new product on the market is safe for consumers in all 31 countries of European Union. It also verifies that marketing claims, written on the packaging, are justified.<\/p>\n

Typically, we receive a lot of demands for new aerosols, but this bit remains dark or unknown for a majority of our contacts. It is a binding key step for any company from a financial and legal perspective. A new product with an incomplete product file exposes itself to the withdrawal from the market.<\/p>\n

This article is particularly relevant for people looking after new products, or modifying existing formulas.<\/p>\n

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What are the steps in this process ?<\/h2>\n

Firstly, the responsible person for the marketing authorisation has to make a notification on the CPNP portal ( i.e. CPNP = Cosmetic Products Notification Portal). This is a must before going any further on the marketing authorisation. This allows the relevant authorities the surveillance and analysis of the market, the evaluation of the products and its information to consumers.<\/p>\n

Then, a big part of the work comes with the next step. The security of a cosmetic product is evaluated and proven thanks to the Product Information File or PIF.<\/p>\n

One of the PIF critical point is the checking of the following materials: CMRs (cancerogen, mutagen, reprotoxical), nanomaterials. (They have to be declared also in the CPNP notification).<\/p>\n

Tests in laboratory are done specifically for marketing authorisation of the product. The analysis and restitution of these tests is very detailed.<\/p>\n

In the facts, these are the regulatory essentials for launching and for the marketing authorisation of a new product.<\/p>\n

What\u2019s the structure for the PIF ?<\/h2>\n

There is an expected structure to respect, and it looks like that:<\/p>\n

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