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Echo Cao
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Articles (92)
Singapore Alerts Mercury-containing Cosmetic Products
Jul 24, 2013
During post-market surveillance, two cosmetic products, Melati UV-Whitening Vit. E Cream and ESTHER Bleaching Cream (A) and (B), are detected to contain mercury by Health Sciences Authority (HSA) of Singapore.
Singapore
Post-market Surveillance
Kanebo Skin-whitening Products are Recalled across Asia, except Chinese Mainland Market
Jul 05, 2013
Kanebo, one of the largest cosmetic giants in Japan, has announced on 4 July that 8 sub-brands covering 54 skin-whitening products containing the ingredient “Rhododendrol” will be recalled across Asia, for being suspected with causing discoloration.
Post-market Surveillance
CFDA Consults on a New Cosmetic Ingredient: Elaeagnus Mollis Deil Oil
Jul 05, 2013
CFDA is inviting public comments on the to-be-approved new cosmetic ingredient, Elaeagnus Mollis Deil Oil, extracted from the fruit of Elaeagnus Mollis.
Chinese Mainland
Ingredients
7 Hospitals in Beijing Selected to Deal with Cosmetics Adverse Effects from July
Jun 26, 2013
According to Beijing FDA, 7 hospitals in Beijing have been entrusted to monitor and deal with adverse effects of cosmetic products from next month. This is just the first batch selected among hospitals having professional dermatology departments and at least 15
Chinese Mainland
Post-market Surveillance
CFDA Approves Test Methods for Prohibited and Restricted Substances in Cosmetics
Jun 07, 2013
On 25 May, China Food and Drug Administration released test methods for a batch of substances prohibited and restricted in cosmetic products, aiming to further standardize requirements for cosmetics testing and enhance the safety and quality of cosmetics.
Chinese Mainland
Ingredients
Testing
Registration of Imported Non-special Use Cosmetic Products in China decentralized to Provincial FDA
May 27, 2013
In the past few years, rumors have that China is intended to lower the regulatory barrier for cosmetic registration and alleviate the heavy pre-market application burden of cosmetic companies but to intensify the post-market supervision and increase enterprises’ sense of responsibility for safety of commercially-available cosmetic products.
Chinese Mainland
Pre-market Approval
Practical Guide to the Registration of New Cosmetic Ingredients in China
May 20, 2013
From 2008 to 2012, 4 years has witnessed merely 3 new cosmetic ingredients approved by CFDA in spite of the continued submission of application dossiers. According to statistics from CFDA, more than 130 dossiers have been submitted for the administrative licensing of NCIs, while most of which are never heard back since.
Chinese Mainland
Ingredients
CFDA Finalized the Second Batch of Existing Cosmetic Ingredients in China
May 14, 2013
On 10 May, China Food and Drug Administration (CFDA) released the Announcement 2 of 2013 to finalize the second batch of the Inventory of Existing Cosmetic Ingredients in China (IECIC), which contains 411 substances in total.
Chinese Mainland
Ingredients
Taiwan Streamlines Registration Documents for Some Medicated Cosmetics
May 09, 2013
From 1 July 2013, manufacturers and importers of medicated cosmetics can submit less technical documents for examination and registration of their products on the condition that
Taiwan, China
Pre-market Approval
CFDA Consults on Testing Methods for Prohibited or Restricted Subs in Cosmetics
Mar 28, 2013
On 15 Mar 2013, China’s CFDA started to invite public comments on the testing methods for some prohibited and restricted substances in cosmetics, including 15 nitroimidazoles and 27 UV filters.
Chinese Mainland
Ingredients
Testing
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