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NEWS
Japan Revise Standards of Quasi Drug Ingredients 2006
Apr 12, 2018
Japan has published the revision to the Standards of Quasi Drug Ingredients 2006. The revision includes amendments to 14 testing methods, 9 existing ingredients standards and the addition of 7 new ingredient standards. This revision has been effective since Mar 29, 2018. Stakeholders have been given a grace period of over 1 years which will end on Sep 30th, 2019. Within this period previous compliance requirements will apply. The revised 14 testing methods are as follow...
Japan
Ingredients
NEWS
Japan Releases Two Instructions on Medicated Soap Market Access Requirements
Apr 09, 2018
Japan MHLW released two instructions for medicated soap market access requirements on Mar 29, 2018. The first instruction regulates the basic requirements for application of medicated soap marketing approval. The second instruction indicates the detailed information on how to fill out the marketing license application form. Requirements for Application for Marketing Approval of Medicated Soaps According to Pharmaceutical and Medical Devices Law, medicated so...
Japan
Pre-market Approval
Ingredients
NEWS
Japan Revised Requirements of Additives Used in Permanent Wave Products and Hair Dyes
Feb 06, 2018
Japan revised the list of additives in permanent wave products and additives in hair dyes. 1. In Hair Dye list, the ingredient "Isostearoyl Hydrolyzed Collagen Solution (2)" (No. 0133) is deleted...
Japan
Ingredients
NEWS
2017 Japan Revision of Collections of Quasi-drugs Additives Standards
Dec 26, 2017
Japan has appended and revised quasi-drug additive standards to include approved additives for quasi-drugs which haven't been listed on "Standards of Quasi-drug Ingredients 2006". The aim is to accelerate application review which is a prerequisite to quasi-drug manufacturing and marketing. Japan issued a “Collections of Quasi-drugs Additives Standards” in 2016. In 2017, the Collection has been revised twice as follows...
Japan
Ingredients
NEWS
2017 Japan Revisions of Positive List of Additives in Quasi-drugs
Dec 26, 2017
In 2017, the positive list of additives in quasi-drugs has been revised several times. Detailed contents are specified here: Revision of 2017.9.19: For number 1124 "Di(Isostearyl /Phytosteryl ) Dilinoleate", add "formulation example" to column (3) "other medical cosmetic products, anti-odor control agents, repellents" in...
Japan
Ingredients
NEWS
Japan Corrected the Error on the Positive List of Additives in Quasi Drugs
Nov 02, 2017
Japan officially admitted a concentration limit error on the Positive List of Additives in Quasi Drugs, and corrected it as...
Japan
Ingredients
NEWS
Japan Released Amendment of Standard of Quasi Drug Ingredients 2006
Apr 18, 2017
Japan MHLW revised its overall standards for raw ingredients used in quasi drug on Mar 30, 2017. The amendment mainly refers to general testing methods changing of some items and quality standard modification of several ingredients...
Japan
Ingredients
Safety Assessment
Testing
NEWS
Japan Adjust Concentration Limit of Fluoride Used In Medicated Toothpaste
Apr 13, 2017
The permitted maximum concentration of fluoride used in medicated toothpaste (except for liquid form) in Japan has been raised to 1500ppm (previously 1000ppm). Toothpaste with fluoride (concentration surpass 1000ppm and below 1500ppm) will be treated as a quasi drug. For toothpaste with more than 1000ppm...
Japan
Ingredients
NEWS
Japan Publish English Translation of Revised Quality Standard of Permanent Wave Agent
Apr 10, 2017
Japan Ministry of Health, Labor and Welfare (MHLW) published the whole English translation of revised "Standard for Marketing Approval of Permanent Wave Agent" with attached "Qality Standard of Permanent Wave Agent". MHLW amended..
Japan
Pre-market Approval
Ingredients
NEWS
Japan Bans 19 Ingredients for Use in Medicated Soaps
Oct 09, 2016
Japanese Ministry of Health, Labour and Welfare (MHLW) announced the ban of 19 kinds of ingredients for use in medicated soaps including medicated hand wash, medicated shower gel and medicated facial cleansing.
Japan
Pre-market Approval
Ingredients
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[Updated] EU Adopts 11 Changes to the Use Requirements for Cosmetic Ingredients
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[Updated] EU Finalizes Amendments to Use Restrictions on D4, D5, D6 in Cosmetics
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China Consults on Guidelines for Submission of Cosmetic Safety Assessment Dossiers: Exemptions for Two Types of Cosmetics from Safety Assessment Report Submission
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[Updated] Taiwan Amends the List of Prohibited Ingredients in Cosmetics
Featured
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Stay Current: China’s Cosmetic Safety Assessment Regulatory Landscape
Under the current regulatory framework, cosmetics registrants and notifiers can continue to submit a simplified version of the safety assessment report during the registration or notification process until May 1, 2025. Following this deadline, a full version of the safety assessment will be mandated. To facilitate a smooth transition, China is planning to release a set of technical guidelines.
China’s Safety and Technical Standards for Cosmetics (STSC) and Its Updates
The current cosmetic technical standard STSC 2015 specifies the cosmetics' general safety standards, prohibited/restricted/permitted ingredients and testing methods. It is revised aperiodically in response to changing trade practices in the industry. China is planning to issue a new version of STSC.
Cannabis Cosmetics Regulatory Updates in the Asia Pacific Region
Cannabis cosmetics are undoubtedly one of the hottest products across the globe in recent years, but with few regulations. To assist cosmetics companies to avoid compliance risks and seize market opportunity, ChemLinked has compiled the regulations.
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