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ECHA Publishes Microplastics Reporting System Requirements under REACH

On April 16, 2025, the European Chemicals Agency (ECHA) published detailed requirements for the reporting of synthetic polymer microparticles, commonly referred to as microplastics, under the REACH Regulation. This initiative aims to enhance transpar

ANMAT Modernizes Import Rules for Medical Devices, Cuts Minimum Shelf Life Requirement to Six Months

In a move welcomed by the healthcare and medical technology sectors, Argentina’s National Administration of Drugs, Food and Medical Technology (ANMAT) has issued a new Disposition that reduces the minimum shelf life required for imported medical de

South Korea Notifies WTO of Proposed Amendments to Medical Device Regulation

On May 9, 2025, South Korea notified the World Trade Organization (WTO) of proposed amendments to the "Regulation on the Permission, Notification, Review, etc of Medical Devices”. The revision aims to clarify cybersecurity documentation requirement

EU Adopts New Restrictions on UV-328 and Dechlorane Plus Under POPs Regulation

In May 2025, the European Commission adopted two Delegated Regulations introducing new restrictions under Regulation (EU) 2019/1021 on Persistent Organic Pollutants (POPs). These measures implement decisions from the Stockholm Convention and target t

An Introduction to K-REACH or Korea REACH

The Act on Registration and Evaluation, etc., of Chemical Substances (ARECS), commonly known as K-REACH, managed by South Korea’s Ministry of Environment (MoE), is a key chemical regulation that ensures the safe management of chemical substances. K

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