Recent in Updates by Region (page 10 of 12)

Canadian Regulatory Update

Discussion of regulatory changes, beginning with the most urgent. In addition, highlights comments published by Health Canada, in conjunction with Advertising Standards Canada, on acceptable and unacceptable cosmetic claims.

The FDA's 'Wish List': A Unified Agenda

The Regulatory Flexibility Act of 1980 and Executive Order 12866 require the publication of a semiannual inventory of the rulemaking under development, and the US Department of Health and Human Services (HHS) publishes this wish list for the FDA. The latest came out on Dec. 7, 2009.

Recent ATPs and the 8th Amendment

Why does the Cosmetic Directive need the 8th Amendment? Some feel it is necessary since the directive has been changed 55 times, including seven amendments and 48 Adaptations to Technical Progress (ATPs). While the industry waits to see what this new amendment will bring, more ATPs have been published, as are described here. Science moves on contrary to political wishes.

EU Update—Changes with Implementation of 1223/2009

The implementation of Regulation 1223/2009 is of prime importance to the cosmetics industry. Although many requirements remain the same as in the directive, there are changes that will have an impact on companies, with compliance required by July 11, 2013.

Myanmar Cosmetic Regulations

Myanmar is a member state of the ASEAN community and must abide by ASEAN Cosmetic Directive; however, like other member states, it has local regulatory bodies such as the Ministry of Health that supervise goods sold in the country.

US and Canada Regulatory Updates

Several major regulatory changes are coming in cosmetics from Canada, while in the United States, the U.S. Food and Drug Administration (FDA) has been active in sending out warning letters to cosmetic companies making unapproved drug claims. This column provides an overview of them.

Asia-Pacific Update: ASEAN Updates to Nano, Sun Care, Trace Limits and More

Changes to the European Union’s Cosmetic Directive 76/768/EEC were a main topic of discussion at the meeting of the ASEAN Cosmetic Scientific Body (ACSB) and the ASEAN Cosmetic Council (ACC), which took place in Cambodia on July 11-12, 2012.

Cosmetic Control Unit in Singapore

In 2008, Health Sciences Authority (HSA) established the ASEAN Cosmetic Directive (ACD) for cosmetic products in Singapore. This is enforced as the Heath Products Act, a subsidiary legislation of the HSA’s Health Products Regulation 2007. The HAS set up the Cosmetic Control Unit of Singapore to regulate cosmetics.

Korean Cosmetic Regulations

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.

PCPC Meeting Focuses on Innovation, Global Growth, Legislative Efforts, Digital Technology

Speakers at the event included Council president and CEO Lezlee Westine and Council chairman and Elizabeth Arden CEO and president Scott Beattie, and topics included social media efforts, collaborative partnerships, marketing solutions and more.

EU Update—Changes with Implementation of 1223/2009

The implementation of Regulation 1223/2009 is of prime importance to the cosmetics industry. Although many requirements remain the same as in the directive, there are changes that will have an impact on companies, with compliance required by July 11, 2013.

Myanmar Cosmetic Regulations

Myanmar is a member state of the ASEAN community and must abide by ASEAN Cosmetic Directive; however, like other member states, it has local regulatory bodies such as the Ministry of Health that supervise goods sold in the country.

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