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2023.03
What information does the electronic cigarette PMTA need to submit? The key information to be submitted by PMTA is as follows: Only enterprises that have successfully applied for FDA can apply for PMTA.
What supervision does FDA have on electronic cigarette manufacturers? Manufacturers in the United States need to register every tobacco production site in the factory with FDA and report any harmful substances and potential harmful substances.
What are the requirements for electronic cigarette manufacturers to export to the United States? The FDA of the United States requires all electronic cigarette products sold in the United States market to submit an application for ingredient list.
The structure of electronic cigarette is mainly composed of cigarette rod and cigarette oil. The entry of electronic cigarette into the United States market needs to consider the safety certification UL certification and FDA test.
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The TPD of EU countries and the MHRA registration fee of the UK. The Tobacco Product Directive (TPD) is used to regulate and supervise the manufacturing, sales, display (product design, packaging, etc.)
What is VCCI certification? VCCI is the EMC certification mark of Japan and is managed by the Japan Electromagnetic Interference Control Committee. VCCI certification is not mandatory.
What is TELEC certification? The Japanese TELEC certification is called the Japanese radio wave method, also known as the MIC certification, which is the certification for radio frequency equipment in Japan.
METI filing is a regulation of Japan's DENTORL Law (Electrical Equipment and Material Control Law), which requires Japanese purchasers to register with Japan METI within one month after purchasing goods within the scope of PSE certification.
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What are the benefits of REACH testing in the EU? REACH testing will ensure a high level of protection for health, safety and environment, and ensure that the EU internal market plays an appropriate role in the field of chemicals;
It is required to register the basic information of all existing and new chemicals and chemical substances used in various products with an annual output of more than 1 ton. Only registered substances can be produced or imported into the EU.
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