What is the process of registering cosmetic products in the Spanish market.

What is the process of registering cosmetic products in the Spanish market.
Under Project LARGO, Switzerland has overhauled its food and consumer product regulations, harmonizing them with current EU laws and standards.
Do cosmetics products sold online need to comply with EU regulations? Of course! Products sold online within the EU are fully covered by all EU regulations.
The Obelis' team break down and explain the European CE marking process and the steps required in obtaining a CE mark for a product or device on the EU market.
EU vote confirms cranberry products are not medical devices. This is the first borderline product ruling adopted based on MDD 13(1)(d).
EU regulations require a European Responsible Person be designated for products to be registered and placed on the EU market by any non-EU manufacturer.
Several Opinions were recently issued by the Expert Committees in regard to the use of fragrances in cosmetic products, as serious concerns were raised over their allergenic potential.
The new EU Medical Devices Regulation 2017/745 (MDR) officially entered into force on 25th May 2017 amending the Directive 93/42/EEC and will be fully applicable after a transition period of three years (2020). One of the most relevant changes introduced by the new Regulation lies in the extension of its scope, now including certain “products without an intended medical purpose”.
Silicones like Cyclopentasiloxane (D5) and Cyclotetrasiloxane (D4) have been restricted in cosmetics products. Read about the major changes here.
One of the key requirements towards cosmetic products is their safety for human health. Find out what evaluates the stability testing.