Philippines FDA announced the pilot implementation of the Automatic Notification of certain cosmetics, through which pilot products can automatically obtain a CPN via FDA ePortal system.
- Home
- /tags
tags
Cosmetics
CIRS Group has compiled and summarized the latest global cosmetics regulatory developments in August 2026.
Learn what brands need to know when launching sunscreens in the EU, UK, and China. This practical guide covers sunscreen classification, permitted UV filters, SPF and UVA testing requirements, labeling, and key regulatory differences to help companies plan compliant global sunscreen launches and avoid costly delays.
South Korea launched the “Cosmetic Safety Assessment Support” website to provide support for the cosmetic safety assessment system that will be phased in from 2028.
Not all cosmetic test reports are created equal: some are rejected by regulators, and some aren’t internationally recognized. Choosing the wrong laboratory can delay your product launch or even block market entry entirely. This article explains the differences between CMA, CNAS, and ISO 17025 accreditation, why they matter for cosmetic testing in China, and how to select the right lab for regulatory compliance.
On June 10, 2026, South Korea MFDS published the "Guide for Preparation of Cosmetic Safety Assessment Documentation" , providing guidance for cosmetic responsible distributors on preparing safety assessment documentation.
On May 29, 2026, China’s National Medical Products Administration (NMPA) released eight testing methods to be incorporated into the corresponding chapters of the Safety and Technical Standards for Cosmetics (2015 Edition).
On April 20, 2026, the Korea Cosmetic Association (KCIA) issued Notice No. 4-161, forwarding document No. 2757 from the Ministry of Food and Drug Safety (MFDS) Cosmetic Policy Division. The notice announces a legislative proposal initiated by Representative Baek Jong-heon to partially amend the Cosmetics Act, and invites public comments. The core objectives of the proposed amendment are to strengthen regulatory measures against the sale of "IP-infringing cosmetics" and to establish an export support mechanism. The KCIA feedback deadline is April 23, 2026.
On April 13, 2026, China’s National Medical Products Administration (NMPA) carried out the fourth dynamic adjustment to the Inventory of Existing Cosmetic Ingredients in China, involving a total of 50 records. For certain ingredients revised in IECIC I, the updated names differ from those currently listed in the EU Cosmetic Ingredient Catalogue ((EU) 2025/1175) and the US INCI database.
Health Canada is implementing new regulations that will require cosmetic manufacturers to disclose specific fragrance allergens directly on product labels, marking a shift from current practices that allow fragrance ingredients to be listed collectively under "parfum" or "fragrance."
