Understanding the Compliance Requirements for Cosmetics and Health & Beauty Products
Intertek is pleased to help our clients bring their cosmetics and health & beauty products to market. To enhance our commitment to these industries, we invite you to attend our free webinar series on a variety of regulatory compliance and testing considerations.As experts in providing compliance services, our Cosmetic Team has extensive experience in global cosmetic regulations. In addition, our team consists of knowledgeable specialists with strong academic backgrounds, such as toxicology, chemistry, pharmacy and medicine and are actively involved with technical and trade associations. During the webinars, our presenters will share their experiences and interpret the requirements from the aspects of product formulation, testing, labels, claims, as well as, address the continually changing regulatory landscape for cosmetics and the challenges it presents to stakeholders.
This webinar will be presented in French.
Après la mise en place du règlement CLP CE N°1272/2008 (Classification, Labelling and Packaging), l’harmonisation au niveau Européen des déclarations aux centres anti poison est un sujet incontournable. Actuellement les déclarations se font dans chaque pays de mise sur le marché où les règles divergent d’un pays à l’autre.
A partir du 1er Janvier 2020, tous les produits classés comme dangereux pour la santé ou présentant un danger physique seront à déclarer. Les déclarations seront à faire selon un format harmonisé via le Poison Centres Notification (PCN) portal. De nouveaux éléments entrent également en application, l’UFI (Unique Formula Identifier) et EuPCS (European product categorisation system).
Quelles sont ces nouvelles exigences ? Comment vous y préparer ? Nos experts vous proposent un point à date des exigences en France et de la mise en place au niveau Européen des déclarations aux centres anti poison. Ce webinar s’adresse aux importateurs et aux utilisateurs en aval qui mettent sur le marché des produits chimiques soumis au règlement CLP et aux Fiches de données de sécurité (FDS), par exemple : Parfums d’ambiance, bougies, aérosols, peintures, colles, encres, détergents, matières premières…
Recorded: Nov 8, 2018
This webinar will focus on the use of advanced analytical, chemical and materials expertise to address areas of keen interest to those in the Health and Beauty products space. Through a variety of case studies, the following areas will be explored - source and level of impurities in finished products, product performance claim development, maintain brand integrity by rooting out counterfeit products and ensure compatibility of packaging with their products.
Recorded November 27, 2018
Oral care personal care products which are classed as cosmetics in certain global regions such as Europe benefit from in vitro testing to help accelerate product development and support marketing claims. Novel oral care products need to be safe for use by consumers and must also perform well and whilst in vivo clinical studies for oral care products are the gold standard in terms of product assessment, these can be rather complex, time-consuming and expensive. Instead, a well-designed in vitro test can often yield the required data much more quickly and at a lower cost.
In this webinar session our expert, Pete Hall, will introduce in vitro study approaches for oral care products and illustrate with several case studies how such studies – whether they are to support early-stage development of a product formulation or in support of marketing claims or pack claims - may accelerate product development.
Recorded: January 24, 2019
Cosmetic products that have medicinal or drug-like benefits, otherwise known as cosmeceuticals, must be substantiated for safety before going to market, which involves analytical chemical analysis to verify active ingredient content and the absence of hazardous materials. Cosmetic companies know that consumer safety is the number one priority, so they invest resources in scientific research and testing to ensure their products are safe and compliant with the laws and regulations and they can also support their all-natural claims.
This webinar focuses on the types of chemical analysis performed and methods used to identify the presence and quantity of active ingredients, additives or harmful materials in cosmeceuticals and all-natural products. We will also discuss the importance of why manufacturers, suppliers and retailers should understand what is in their cosmetic products to mitigate sources of risk across the supply chain.
Recorded January 31, 2019
Since November 10, 2018, a national unified record-keeping management system for first-time importation of non-special use cosmetics has been officially implemented in China. In light of this recent amendment, we will provide a recap of the basic notions and regulatory requirements of cosmetics in China with a special focus on the new record-keeping management system and Chinese Responsible Person.
This webinar will be in French.
Recorded January 31, 2019
Depuis le 10 novembre 2018, un système national de gestion des enregistrements a été officiellement mis en place pour la première importation des cosmétiques « non-special use » en Chine. Suite à cet amendement, nous rappellerons les notions de base et les exigences réglementaires en matière de produits cosmétiques en Chine, avec un focus sur le nouveau système des enregistrements et la Personne Responsable en Chine.
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