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New in Regulatory (page 5 of 45)
Jan 23, 2012 | 10:36 AM CST
China Suggests Eight Categories for Licensing Special Use Cosmetics
China's State Food and Drug Administration (SFDA) sought comment regarding its recent organization of "special use cosmetics" into eight different categories. On Dec. 29, 2011, the SFDA published eight draft categories to obtain a hygienic license including: liquid, half solid, solid, cream or lotion, aerosol, organic solvent, ceryl-based and other.
Jan 11, 2012 | 11:43 AM CST
Advocacy Groups File Suit Against the FDA Over Nanotechnology Regulation
A coalition of six consumer safety and environmental groups is suing the US Food and Drug Administration (FDA) over its lack of nanotechnology regulation, specifically for sunscreen.
Jan 09, 2012 | 02:39 PM CST
Challenges in Sun Care Formulating
By: Rachel L. Grabenhofer
Sun care formulating poses several challenges to product developers. Cosmetics & Toiletries recently asked, “What are the biggest challenges in sun care formulating?” Following are your responses.
Jan 05, 2012 | 04:29 PM CST
Regulatory Review—Canadian Update
By: David C. Steinberg, Steinberg & Associates
Canada has had many regulatory changes to its chemicals, drugs and most recently, to its cosmetics. This column will discuss those regulatory changes, beginning with the most urgent. In addition, this column will highlight new comments published by Health Canada, in conjunction with Advertising Standards Canada, on acceptable and unacceptable cosmetic claims.
Jan 05, 2012 | 03:06 PM CST
Asia-Pacific Update: Korean Cosmetic Regulations
By: To Yo Be, Contributing Author and Consultant
In Korea, cosmetics and related products such as foods, food additives and pharmaceuticals are regulated by the Korea Food and Drug Administration (KFDA). The Korean Cosmetic Products Act (KPCA), which was passed in 2000 to separate cosmetic and pharmaceutical regulations, categorizes cosmetic products into three major categories: general cosmetics; functional cosmetics, e.g., sunscreens and whitening products; and quasi drugs, e.g., anti-acne products.
Nov 29, 2011 | 02:01 PM CST
Researchers Suggest Gluten Identification in Cosmetics
Research presented at the American College of Gastroenterology’s (ACG) 76th Annual Scientific meeting in Washington, D.C., USA, suggested that celiac patients may have adverse reactions to gluten in cosmetics.
Nov 21, 2011 | 03:17 PM CST
Updates Encouraged for Health Canada's In-Commerce List
By: David C. Steinberg, Steinberg & Associates
Suppliers that export chemicals directly into Canada or that supply ingredients for finished products that are sold in Canada and, therefore, regulated under the Food and Drugs Act (F&DA) in Canada need to ensure that these substances are nominated to the revised In-Commerce List (ICL) in Canada.
Oct 28, 2011 | 01:42 PM CDT
Silicone Safety and the Cosmetic Industry
By: James Lambert, PhD NuSil Technology LLC
The use of silicones in personal care products continues to expand because of the unique performance attributes they provide and their well-established record of safety. As a result, progressively larger volumes of silicones are being released to the environment, and interest in their life cycle has increased. The present article summarizes relevant fundamental chemical and physical properties of silicones and how these relate to material performance, safety and environmental fate.
Oct 28, 2011 | 01:32 PM CDT
Changes to US Sunscreen Regulations
By: David C. Steinberg, Steinberg & Associates
The newest regulations and comments on sunscreens from the US Food and Drug Administration (FDA) were officially published in the Federal Register on June 17, 2011, and will go into effect June 17, 2012.
Oct 19, 2011 | 04:20 PM CDT
EU Regulatory Update: The Individual Safety Assessment–a Practical Approach towards Regulation (EC) No 1223/2009
By: Annelie Struessmann, PhD, CONUSBAT
The new Cosmetics Regulation (EC) No. 1223/2009 defined the format of the Cosmetic Product Safety Report (CPSR) in the Regulation’s Annex I. Accordingly, the information for documenting the product’s safety is to be listed in a part A of the CPSR, and this needs to include the toxicological profiles of the ingredient substances, their physical and chemical characteristics, impurities, trace components, as well as their exposure criteria in use.
