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Section: Regulations > Regional

Importing Cosmetics into Japan: Part 1

This column is the first in a two-part series on importing cosmetics into Japan. It discusses the general requirements for cosmetic manufacturers and distributors. The second part discusses these requirements in more depth, and provides a closer look at sunscreen requirements.

Importing Cosmetics into Japan, Part 2: Distributor Licensing and Sunscreens

This column is the second in a two-part series on importing cosmetics into Japan. It discusses the requirements for cosmetic manufacturers and distributors in more depth than the first part, and provides a closer look at sunscreen requirements in Japan.

The Innovation Zone at in-cosmetics 2013 in Paris.

Formulating New Beauty at in-cosmetics 2014

in-cosmetics 2014 (Hamburg Messe Germany, April 1-3) puts formulating in the spotlight while uncovering the most important industry trends and developments for 2014 and beyond.

Challenges in Creating NPA- and WFM-compliant Natural Formulations

Where does the formulation chemist begin when facing a marketing request for a product stamped with a “natural” label claim? The first step is to identify the certifying organization or government under which the formulation is to be sold, followed by the choice of preservatives. The basic approach to composing natural products is outlined here.

Nanoparticles in Sunscreens: Fact and Fiction

This paper reviews important issues regarding the classification for UV active ingredients and the need for a uniform classification and labeling system covering all nano ingredients. The definition of nanoparticles is not questioned here; however, the highly selective manner in which the definition is applied to different materials is.

Cosmetic Notification in Brunei

Cosmetics in Brunei are regulated by the country’s “Medicines (Cosmetic Products) Regulations 2007,” which are in line with the ASEAN Cosmetic Directive (ACD) and require all importers/ manufacturers to notify the Ministry of Health (MoH) before launching any cosmetic product in the local market.

Nanoparticles in Sunscreens: Fact and Fiction

This paper reviews important issues regarding the classification for UV active ingredients and the need for a uniform classification and labeling system covering all nano ingredients. The definition of nanoparticles is not questioned here; however, the highly selective manner in which the definition is applied to different materials is.

The Cosmetics Industry: Still Going After a Thousand Cuts

I have been in the cosmetics industry for nearly 45 years, and for 18 of them, I have written about regulations for Cosmetics & Toiletries magazine. Sadly, this will be my penultimate column, and a reflection of my time in the industry.

FDA Rule for Broad-spectrum Labeling: Key Substrate Findings

UVA protection is part of the mandatory testing for claiming broad-spectrum sun protection. A worldwide standardization is in development with the ISO TC217, expected for UVA testing 2012. The FDA has issued a final rule following Colipa’s proposed UVA in vitro method. While this rule establishes UVA labeling and testing, inconsistencies remain. This study compares the critical wavelength in roughness and application before and after two levels of UV doses.

Keeping Cosmeceuticals Cosmetic

Global demand for cosmeceuticals continues at an explosive rate and the discovery of antiaging medical interventions, coupled with new functional active ingredients, provides a fertile innovation ground for product developers. This paper discusses current scientific and regulatory affairs to take into consideration for the successful commercialization of cosmeceutical products.

Canada, California and Congress: The Three C’s of New North American Regulatory Concern

On April 26, 2008, Canada released new Volatile Organic Compounds (VOCs) requirements. These requirements are aligned with the current California Air Resources Board (CARB) requirements in which companies that emit VOCs are required to register and maintain VOC records for five years.

The EU's Proposed 8th Amendment

Just as the industry began to comply with the 7th Amendment to the Cosmetic Directive, the European Union (EU) Commission proposed the new 8th Amendment. After confusion surrounding the old rules, the commission attempted to correct matters, only making them worse.

Six Common Criteria for Cosmetic Claims in the EU

In European Cosmetics Regulation No. 1223/2009, the European Commission (EC) has chosen to regulate cosmetic claims in addition to the existing regimes, saying that consumers should be protected from misleading claims concerning efficacy and other characteristics of cosmetic products.

Harmonizing Cosmetics Standards: ISO

The importance of harmonization continues to grow. Past and present standard-setting work by ISO, such as in microbiology and sun protection, is laying the foundation for future bridges across regulatory gaps.

Regulations in ASEAN Countries

The Association of Southeast Asian Nations (ASEAN) has agreed to harmonize its cosmetic regulatory scheme.

Testing Tactics: REACH and In vitro Alternatives: Skin Irritation Testing

Welcome back to a continuing discussion regarding the new Registration, Evaluation and Authorization of Chemicals (REACH) regulation and its impact on chemical testing. It is the purpose of this series of articles to provide an overview of these existing validated in vitro methods, as well as new methods that are being considered for validation.

Regulatory Review: Australian Regulations Update

Australia issued its new Cosmetics Standard 2007. The following is a breakdown of products originally considered as therapeutic drugs if they made SPF claims, and that will now be regulated as secondary sunscreens.

The poster exhibition at the Sun Protection Conference 2013

Sun Protection Conference Addresses the Future of Sun Care

The conference opened the summer season for sun care scientists, and the topics included SPF and UVA standard tests, new sunscreen actives, greater product efficacy and improved product textures.

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