Based on the compliance requirements of the EU Extended Producer Responsibility (EPR) and the guiding framework for environmental protection systems, different EU countries/regions have gradually developed their EPR systems to identify [...]
Green Circle Speaks Cross-Border] - German EPR Policy Compliance Interpretation Read More »
EU Energy Efficiency Label: EU Authorized Representative Information: In accordance with the EU Market Surveillance Regulation and Implementation Guidelines, which came into force on July 16, 2021, the principal place of business is
PPE Introduction: PPE: Personal Protective Equipment, PPE is the English abbreviation for Personal Protective Equipment.
Green Circle Talks Cross-border]-EU PPE Commodity Compliance Interpretation Read More »
First, what is children's pajamas Children's pajamas, refers to the main use of sleep or sleep-related activities when wearing clothing products, such as tops pajamas, one-piece pajamas, robes and so on.
Green Circle Speaks Cross-Border] - U.S. Children's Pajamas Compliance Interpretation Read More »
What is an appliance? Electrical appliances refer to all appliances that use electricity. According to the external specific signals and requirements, automatic or manual connection or disconnection of the circuit, continue or continuous change of
A: In recent years, more and more exporters of beauty and hospitality products have set their sights on the Saudi market in the Middle East, and their investment in the Saudi market has been increasing day by day. However, due to
I. DEFINITION OF FOOD CONTACT SUBSTANCES ✅Food Contact Substances (FCSs) refer to substances that
The FDA Mark does not represent any legal regulation or certification and its use is strictly prohibited in commerce. By law, the FDA Mark may not be displayed on product packaging, but may only be printed on FDA packaging.
Green Circle Talks Cross-Border] - Can the FDA LOGO be printed on product packaging? Read More »
The U.S. Food and Drug Administration's (FDA) regulatory work is a complex and rigorous process designed to protect public health and ensure the safety of food, drugs, and other commodities.
Canning refers to the process of sealing food products in containers such as cans, jars, semi-rigid packages or soft packages. In the past, due to insufficient heat treatment or acidification, canned foods have been canned in a variety of ways.
The FDA's definition of cosmetics does include a range of products that are used in various forms in everyday life for the purpose of cleansing, beautifying, increasing attractiveness, or altering the external
Based on the information you have provided and the provisions of the Modernization of Cosmetic Regulations Act of 2022 (MoCRA), adverse events involved in FDA registration of cosmetic products
In the U.S., electric toothbrushes are categorized as medical device Class I products, and their market entry requires obtaining medical device FDA registration codes and meeting Federal Communications Commission (FC) requirements.
U.S. FDA Definition of a Laser Electronic Product The U.S. Food and Drug Administration (FDA) defines a laser electronic product as any product that contains an electronic circuit capable of emitting a laser light.
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