On January 31, 2020, the UK officially reached a Brexit agreement with the EU, and the Brexit transition period ended on January 1, 2021. Since then, cosmetics entering the UK market must comply with the UK’s regulatory processes and requirements. So, what are the current regulatory requirements, and how should the process be carried out? KASEY […]
Is very important for us know the products you sell in which country. In some countries they are cosmetics regulations will differ. Prior to placing the cosmetic product on the EU market, it is mandatory to notify the product to the EU Commission via the Cosmetic Product Notification Portal (CPNP). CPNP is an EU-wide web-based […]
Animal testing is out of the question at Kasey Beauty. We hereby declare we do not use any ingredients tested on animals and we do not test any of our products on animals. Our commitment to no animal testing is sincere and longstanding. We have never even done business with anyone who practices animal testing […]
If you plan to sell the cosmetics to European, and based on the European regulation (EC) No 1223/2009 on cosmetic products requires industry professionals doing CPSR （ Cosmetic Product Safety Report ）, PIF ( Product Information File ) , CPNP（ Cosmetic Products Notification Portal）for each product commercialized
Finally, each cosmetic product placed on the EU market needs to have a Responsible Person (RP) assigned. The RP has to be based in EU (their address indicated in the label), and their primary task is to guarantee that each cosmetic product placed on the market always remains safe and compliant with the regulation. Their […]
The compliance of the cosmetic product labels with the regulation is very important, as this is the part of the product that is the most prominent and noticeable both for the consumers and for the authorities. The EU Cosmetics Regulation lists very specific requirements for labeling of cosmetic products placed on the EU market. According […]
Manufacturing companies must demonstrate compliance with the good manufacturing practices (GMP) in the PIF. GMP compliance should be in accordance with relevant harmonized standards, the references of which have been published in the Official Journal of the European Union. One internationally recognized GMP standard specific for cosmetics is ISO 22716:2007. Certification provided by third parties […]
One of the legal requirements before placing a cosmetic product on the EU market is to ensure that the product has undergone a safety assessment (part B of the CPSR). CPSR （ Cosmetic Product Safety Report ）is comprised of two parts Part A: Cosmetic Product Safety Information Part B: Cosmetic Product Safety Assessment This means that […]
“All cosmetic products placed on the European Union (EU) market must comply with the EU Cosmetic Regulation (EC) No. 1223/2009. Legislation which has been in force since July 2013. The objective of this new law is to protect consumers. It protects them from potential health hazards and to help them make informed decisions when purchasing […]
A cosmetics selling in the EU must comply with the regulation, and what are the tests need to undergo for cosmetics? We are a manufacturing and trading combo for cosmetics in Yiwu China, with more than 10 years of customizing experience. That is no problem for us to provide legal papers for you. Stability […]
A Product Information File (PIF) must be completed for all Cosmetics intended to be marketed within the EU. What is the Product Information File (PIF)? The European regulation (EC) No 1223/2009 on cosmetic products requires industry professionals to provide a Product Information File (PIF) for each product commercialized. According to regulation 1223/2009 article 2.11, the […]
The CPSR （ Cosmetic Product Safety Report ）is comprised of two parts; Part A: Cosmetic Product Safety Information Part B: Cosmetic Product Safety Assessment. In accordance with Annex I of Regulation (EC) No 1223/2009, Part A of the CPSR is intended to collect the necessary data to justify the safety of the cosmetic product. As a […]
Compliance with good manufacturing practice shall be presumed where the manufacturing process is in accordance with relevant harmonised standards, the references for which are published in the Official Journal of the European Union.
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