It is currently not possible to perform in-depth environmental and health risk assessments of all chemical substances in use in Europe because of the great variety of chemicals and their diverse uses. This Regulation establishes rules to be complied with by any cosmetic product made available on the market, in order to ensure the functioning of the internal market and a high level of protection of human health. 10-Jun-2022. The Regulations on Medical Devices (Regulation (EU) 2017/745) and on In-Vitro Diagnostic Devices (Regulation (EU) 2017/746) changed the European legal framework for medical devices, introducing new responsibilities for EMA and national competent authorities in the assessment of certain categories of medical device. Industrie Cosmetiche Riunite S.p.A. as Data Controller, in order to provide the requested information and will be stored only for a period not exceeding the purposes for which the Data Why is it used in cosmetics and personal care products? This is the second time that Shanghai has revised the regulation after eight years, adding 24 new articles and amending 63 articles. Why is it used in cosmetics and personal care products? The new regulation comes into force on 1 Jan 2021. Specifically, the EU Cosmetics Regulation requires cosmetic products to provide the following information on the label or on the packaging: Regulation (EU) 2017/745 on medical devices becomes applicable in the European Union today, 26 May 2021.. 31 August 2021 The introduction of the full ban on animal testing for cosmetics in the EU in 2013 was unquestionably a pivotal milestone for animal welfare. Confused from all of these words? This Regulation repealed Directives 67/548/EEC and 1999/45/EC as of 1 June 2015. Disodium EDTA and the related ingredients bind to metal ions which inactivates them. 10-Jun-2022. The new regulation comes into force on 1 Jan 2021. Definitions. September 2022; August 2022; All News; Multimedia. (2) This Regulation aims to ensure the smooth functioning of the internal market as regards in vitro diagnostic medical devices, taking as a base a high level of protection of health for patients and users, and taking into account the small and medium-sized enterprises that are active in this sector. Existing SDSs can be used until 31 December 2022. 1. Regulation 1223/2009, Product Information File, safety assessment, labelling and claims, CPNP notification, SCPN notification, IFRA certificate, COA, cosmetic product classification, competent authority, cosmetic product notification, cosmetovigilance, period after opening, PAO, shelf life, technical data sheet, Staphylococcus COSlaw is a project of Obelis Group. Today, when the discussion on animal testing is high on the European agenda again, Cosmetics Europe emphasises its full support for the ban under the EU Cosmetic Products Regulation. Regulations can be distinguished from directives which, at least in principle, need to be transposed into national law.Regulations can be adopted by means of a variety of legislative procedures depending on their subject matter. Why is it used in cosmetics and personal care products? Regulation 1223/2009, Product Information File, safety assessment, labelling and claims, CPNP notification, SCPN notification, IFRA certificate, COA, cosmetic product classification, competent authority, cosmetic product notification, cosmetovigilance, period after opening, PAO, shelf life, technical data sheet, Staphylococcus (2) This Regulation aims to ensure the smooth functioning of the internal market as regards in vitro diagnostic medical devices, taking as a base a high level of protection of health for patients and users, and taking into account the small and medium-sized enterprises that are active in this sector. Cosmetic products must include information that explains what they are for, how to use them safely, and how to obtain the best result. This is the second time that Shanghai has revised the regulation after eight years, adding 24 new articles and amending 63 articles. 1. The newly amended regulations of Shanghai Municipality on the protection of consumers' rights and interests came into effect from August 1st, 2022. cosmetics-prohibited-subs. European Parliament and of the Council is up to date with all changes known to be in force on or before 23 September 2022. Restricted Substances: Annex III, Regulation 1223/2009/EC on Cosmetic Products, as amended by Regulation (EU) 2022/135, OJ L 22 of 1 February 2022 . European Union - 2022/09/01 Draft Commission Regulation laying down ecodesign requirements for mobile phones, cordless phones and slate tablets pursuant to Directive 2009125EC of the European Parliament and of the Council and amending add reference to the revised Ecodesign Regulation on standby, networked standby and off mode This is the second time that Shanghai has revised the regulation after eight years, adding 24 new articles and amending 63 articles. September 2022; August 2022; All News; Multimedia. Ethylhexylglycerin is an alkyl glyceryl ether.This means that the ethylhexyl group is bound to glycerin at one end by an ether linkage. The following product categories hold the largest share of the European market: skin care (23.2 billion) and toiletries (20.6 billion), followed by hair-care products (14.4 billion), fragrances/perfumes (11.9 billion), and decorative cosmetics (9.8 billion) *. Details: (2) Directive 88/378/EEC is based on the New Approach principles, as set out in the Council Resolution of 7 May 1985 on a new approach to technical harmonisation and standards (4).Thus, it sets out only the essential safety requirements with regard to toys, including the particular safety requirements regarding physical and mechanical properties, flammability, chemical This is a legislation item that originated from the EU. Definitions. REACH regulation aims to improve the protection of human health and the environment from the risks that can be posed by chemicals. draft regulation will be discussed for the first time with the Member States in the REACH Committee on 23 September 2022. For the purposes of this Regulation, the following definitions shall apply: Daily news on cosmetics industry and manufacturers in Europe. Article 2. But evidence indicates that current nano-materials may pose significant health, safety, and environmental hazards. Article 2. BPR regulation aims to improve the functioning of the biocidal products market in the EU, while ensuring a high level of protection for humans and the environment. EU. Although they are also alkyl glyceryl ethers, Batyl Alcohol and Chimyl Alcohol (may also be called Cetyl Glyceryl Ether) have traditionally been used as cosmetic labeling names for these alkyl glyceryl ethers. Regulation 1223/2009, Product Information File, safety assessment, labelling and claims, CPNP notification, SCPN notification, IFRA certificate, COA, cosmetic product classification, competent authority, cosmetic product notification, cosmetovigilance, period after opening, PAO, shelf life, technical data sheet, Staphylococcus 10-Jun-2022. For the purposes of this Regulation, the following definitions shall apply: What Is It? espaol etina dansk Deutsch eesti English (Current language) franais Gaeilge hrvatski italiano Understanding BPR; 31 and 33 of the REACH Regulation. European Union - 2022/09/01 Draft Commission Regulation laying down ecodesign requirements for mobile phones, cordless phones and slate tablets pursuant to Directive 2009125EC of the European Parliament and of the Council and amending add reference to the revised Ecodesign Regulation on standby, networked standby and off mode European Parliament and of the Council is up to date with all changes known to be in force on or before 23 September 2022. Regulation & Safety . This Regulation shall be without prejudice to the competence conferred on the European Agency for the Evaluation of Medicinal Products by Regulation (EEC) No 2309/93, Regulation (EEC) No 2377/90, Council Directive 75/319/EEC(27) and Council Directive 81/851/EEC(28). (2) This Regulation aims to ensure the smooth functioning of the internal market as regards in vitro diagnostic medical devices, taking as a base a high level of protection of health for patients and users, and taking into account the small and medium-sized enterprises that are active in this sector. Definitions. espaol etina dansk Deutsch eesti English (Current language) franais Gaeilge hrvatski italiano GMP ensures that products are prepared in a clean environment and that the products are not contaminated in production. Regulation & Safety . The newly amended regulations of Shanghai Municipality on the protection of consumers' rights and interests came into effect from August 1st, 2022. Specifically, the EU Cosmetics Regulation requires cosmetic products to provide the following information on the label or on the packaging: The bans concern mainly uses of microbeads in cosmetics that are rinsed off after use, where the microplastics are used as abrasive and polishing agents. Industrie Cosmetiche Riunite S.p.A. as Data Controller, in order to provide the requested information and will be stored only for a period not exceeding the purposes for which the Data Regulation 1223/2009/EC on Cosmetic Products, as amended by Regulation (EU) 2021/1902, OJ L 387 of 3 November 2021 . The EU Cosmetics Regulation stipulates that all cosmetics products must be manufactured in accordance with the harmonised standards laid out in GMP, in turn described in the Official Journal of the European Union. Cosmetic products must include information that explains what they are for, how to use them safely, and how to obtain the best result. Regulations can be distinguished from directives which, at least in principle, need to be transposed into national law.Regulations can be adopted by means of a variety of legislative procedures depending on their subject matter. 31 August 2021 The introduction of the full ban on animal testing for cosmetics in the EU in 2013 was unquestionably a pivotal milestone for animal welfare. Good manufacturing practices (GMP) are those conforming to the guidelines recommended by relevant agencies.Those agencies control the authorization and licensing of the manufacture and sale of food and beverages, cosmetics, pharmaceutical products, dietary supplements, and medical devices. The Regulations on Medical Devices (Regulation (EU) 2017/745) and on In-Vitro Diagnostic Devices (Regulation (EU) 2017/746) changed the European legal framework for medical devices, introducing new responsibilities for EMA and national competent authorities in the assessment of certain categories of medical device. Regulation (EU) 2017/745 on medical devices becomes applicable in the European Union today, 26 May 2021.. It is currently not possible to perform in-depth environmental and health risk assessments of all chemical substances in use in Europe because of the great variety of chemicals and their diverse uses. This is a legislation item that originated from the EU. Reference. 31 August 2021 The introduction of the full ban on animal testing for cosmetics in the EU in 2013 was unquestionably a pivotal milestone for animal welfare. Early 28/01/2022; 05/05/2017; Legal act Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU (Text with EEA relevance. Regulation 1223/2009/EC on Cosmetic Products, as amended by Regulation (EU) 2021/1902, OJ L 387 of 3 November 2021 . 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