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Vol. 1485 | 24 Jul 2025

EU Commission Delegated Regulation (EU) 2025/843 adds UV-328 to the POPs Regulation. The unintentional trace contaminant limits of UV-328 effective from Aug 4 2025, and decrease on Aug 4 2027, and Aug 4 2029 to reinforce the application and enforcement.

On July 15 2025, the European Commission published Commission Delegated Regulation (EU) 2025/843 to approve the regulation of UV-328 under Annex I to Regulation (EU) 2019/1021 (POPs Regulation). This regulation was approved as proposed and will enter into force on August 4 2025.

To allow laboratories to improve the accuracy of relevant analytical methods and to ensure their uniform and adequate application, the unintentional trace contaminant limit would decrease as scheduled below. Here is the summary:

Substance

Requirements

Effective Date

UV-328

 CAS No. 25973-55-1

100 mg/kg (0,01 % by weight)

August 4 2025

10 mg/kg (0,001 % by weight)

August 4 2027

1 mg/kg (0,0001 % by weight)

August 4 2029

A link to the Regulation is below:
https://eur-lex.europa.eu/legal-content/EN/TXT/PDF/?uri=OJ:L_202500843

If you have further questions, please contact Dr. Kathy Leung (Kathy.Leung@intertek.com) or Dr. Ben Cheng (Ben.PS.Cheng@intertek.com)

 

Dr. Ben PS Cheng

Technical Manager, Global Softlines

With over 10 years of experience in the testing, inspection, and certification industry, Ben possesses extensive hands-on expertise in quality management and laboratory testing across various consumer product categories, including apparel and footwear. He has provided education and support to buyers and retailers on Restricted Substances Lists (RSL) and Manufacturing Restricted Substances Lists (MRSL), helping them develop effective product safety and compliance programs in line with industry best practices and the evolving legislative and regulatory landscape.

 Email: ben.ps.cheng@intertek.com

Dr. Kathy Leung

Senior Technical Director, Global Softlines

Dr. Kathy Leung has over 20 years of experience in the quality assurance industry, specializing in hazardous restricted substances testing for consumer goods, materials, and chemical formulations. She holds a PhD in Analytical and Environmental Chemistry. Dr. Leung actively contributes to industry standards as a member of LabTAC for AFIRM Group, the RSL Taskforce for AAFA, and the ZDHC Laboratory Advisory Group, sharing her expertise to enhance safety and compliance in the field.

Email: kathy.leung@intertek.com

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