In our last article, Is Your Scalp Healthy? – Scalp Health Evaluation Methods (Part I), we have introduced the evaluation methods for dandruff, sebum levels, and itchiness. In this article, we will continue with the evaluation methods for erythema/papules/pustules and the overall hair status.

On November 5, 2025, the European Chemicals Agency (ECHA) published mapping of PFAS uses, serving as an industry support document for the upcoming public consultation on PFAS restrictions. The mapping systematically outlines PFAS applications across 14 major industrial, professional, and consumer sectors, including battery manufacturing, textiles, electronics, and PFAS production.

On November 3, 2025, China's Ministry of Industry and Information Technology (MIIT) released a notice soliciting public comments on the draft Catalog for Compliance Management of the Restriction of Hazardous Substances in Electrical and Electronic Products (2025 Edition) and the draft List of Applications Exempted from Restricted Substances in the Compliance Management Catalog (2025 Edition). The public consultation period lasts until December 2, 2025.

From small issues like paint peeling off phone cases or fading car buttons to major problems like outdoor equipment rusting and failing or electronic components short-circuiting, these seemingly "worn-out" problems often have a common culprit: environmental aging. Excessive humidity, sun exposure, salt spray corrosion, and high-temperature baking—products face environmental stress in real-world use that is far more severe than we might imagine. How can we predict a product's "anti-aging" capability in advance? Aging tests are a critical reliability assessment method. They simulate or intensify various conditions that a product might encounter in actual use, allowing for a quick evaluation of the durability, stability, and lifespan prediction of materials or products.

November 5, 2025, the European Chemicals Agency (ECHA) officially announced the 35th batch of 1 substance of very concern, bringing the total number of substances on the SVHC list (also known as the Candidate List) to 251. Earlier in October, the Member State Committee (MSC) unanimously agreed during its October meeting to classify this substance as a SVHC.

On June 6, 2025, CIRS Group officially launched the Global Cosmetic Ingredient Regulatory Database--Global CosIng. This database integrates regulatory information on cosmetic ingredients from major markets, including China (Taiwan included), the European Union, the United States, Canada, ASEAN countries, South Korea, and Japan. It is designed to provide enterprises with a one-stop, authoritative, and user-friendly platform for ingredient compliance inquiries, supporting cosmetic companies in global regulatory compliance and product development.

Facial towel products must comply with GB/T 40276-2021 "Soft Towels" and GB 15979-2024 "Hygienic Requirements for Disposable Sanitary Products" standards. As an industry-leading professional testing organization, CIRS Testing understands consumer safety concerns and deciphers the safety code of facial towels from a testing perspective, using scientific data to ensure your "facial cleansing needs" are protected!

On July 31, 2025, in order to further regulate and guide the research and evaluation of sunscreen cosmetics, the Cosmetic Supervision Department under China's National Medical Products Administration (NMPA) organized the National Institutes for Food and Drug Control (NIFDC) to draft two technical guidelines: the Technical Guidelines for the Research of Sunscreen Cosmetics (Trial) (Draft for Comments) and the Technical Guidelines for the Research on Quality Control Standards of Sunscreen Cosmetics (Trial) (Draft for Comments), along with their respective drafting instructions. These documents have been released to the public for consultation.

On October 28, 2025, the European Commission formally adopted Delegated Regulation (EU) 2025/1482, introducing significant amendments to provisions related to polybrominated diphenyl ethers (PBDEs) under the EU Persistent Organic Pollutants (POPs) Regulation (EU 2019/1021).

Medical devices, particularly those that directly or indirectly come into contact with a patient's blood, sterile tissues, or mucous membranes, such as surgical knives, catheters, and implants, must be sterile. If the packaging is damaged or improperly sealed during transportation and storage, microorganisms (such as bacteria and fungi) can infiltrate, leading to contamination of the devices. Using contaminated devices may cause infections and even pose a threat to patients' lives. CIRS Testing offers a comprehensive suite of solutions for sterile packaging of medical devices, including microbiological, chemical, accelerated aging, physical and mechanical property, and transportation testing. This ensures patient safety and helps your products comply with regulations to enter global markets!