Global Regulatory Issues for the Cosmetics Industry by C E Betton

By C E Betton

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Based on a presentation made at the Health and Beauty Aids Regulatory Symposium in September 2006. C. I. ), Global Regulatory Issues for the Cosmetics Industry Vol. 1, 21–33 © 2007 William Andrew Inc. 21 22 Global Regulatory Issues for the Cosmetics Industry In the sections below, I will outline the regulatory system in some of the major export markets of Canada and Australasia. The European Union is covered elsewhere in this book and I will leave that to others. I also address some of the requirements applicable within the US; the state of California for instance, has its own requirements in addition to the general Federal Laws that apply to all.

There is no special labeling for NICNAS approval. Therapeutic goods must also use only approved ingredients. The goods must be included in the Australian Register of Therapeutic Goods (ARTG). Safety and efficacy and good manufacturing practices data must also be included. The time for approval of therapeutic goods is approximately 3–6 weeks. 5 China If you pick up any business magazine or newspaper you will always find a reference to China and its economic changes. Here are some statistics. 3 billion people, the most populous country in the world.

Htm 8. EU (2003) The SCCNFP’s notes of guidance for the testing of cosmetic ingredients and their safety evaluation, 5th Revision. 1 Introduction In the area of regulatory affairs, myths are prevalent, and it is important to have current information about the changing regulatory scene. This involves vastly different areas of the world, and a brief summary herein should give clarity to a few of the diverse issues that exist. Consider that any country that needs a passport to enter is one that has a different regulatory system than the US.

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