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EU BPR Regulations Also Have New Challenges Such As Textiles And Footwear.

2014/4/23 8:24:00 18

EUBPRRegulationsTextilesShoes And Garments

< p > > the world's < a target= "_blank" href= "//www.sjfzxm.com/" > clothing < /a > a target= "_blank" href= "_blank".

< /p >


< p > recently, the BPR regulations have been updated. The contents include: first, approved 6 kinds of bioactive substances and their corresponding uses for the bioactive substances, such as copper glycol, 5- methoxazoline, octanoic acid, decanoic acid, iodine and zinc, which are suitable for biocide products; two, public consultation has been launched for 6 active substances, such as thiacloprid, cyfluthrin, dipyrethroid, BIS morpholine, and so on, and three is the list of frequently asked questions to issue the latest biocide regulations.

The regulation will affect exports of dozens of products such as textile and footwear, involving an export volume of about $2 billion.

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< p > < strong > BRP causes three risks < /strong > /p >


< p > < strong > covers a wide range < /strong > < /p >


< p > this regulation not only has a great impact on the production and export enterprises of sanitary pesticides, but also has great deterrent effect on dozens of products such as kitchenware, a target= "_blank" href= "//www.sjfzxm.com/", leather, /a, footwear, carpets, lotions, textile and garments, home building materials, ceramics, electronic appliances, paint and rubber plastics.

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< p > < strong > procedure complexity < /strong > < /p >


< p > enterprises need to prepare the submission of experimental data, arrange and reserve technical data, make compliance with prescribed dossiers and active substances assessment.

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< p > < strong > expensive, < /strong > /p >


The authorized cost of active substances licensing and biocide products is much higher than the registration fees of REACH regulations, and the number of enterprises participating in data sharing will be reduced and the cost of sharing will be higher if BRP regulations are involved. For example, the administrative cost of the first use type of an active substance will be as high as 120 thousand euros, and the authorization fee for a product will be 80 thousand euros. P

< /p >


The European Union is the largest market for Ningbo's foreign trade. In 2013, our European products exported to Europe reached a record high, with an export volume of US $19 billion 890 million.

According to BPR regulation, upstream and downstream related industries chain is conservatively estimated, with the threshold set by the European Union to less than 2 billion dollars in the whole city.

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< p > < strong > extension > /strong > /p >


< p > EU biocide < a href= "//www.sjfzxm.com/news/index_q.asp" > < /a > (BPR, BiocidalProductsRegulation) was formally implemented in September 1, 2013.

The BPR regulations incorporate the TA (BiocidalTreatedArticle) into the regulatory framework based on the BPD directive, aiming at strengthening the supervision of the biocides disposal products in the EU market.

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< p > < strong > what is biocide handling substance (TA) < /strong > /p >


< p > BiocidalTreatedArticle (TA) refers to any substance, product or article that has been disposed or intended to contain one or more biological products.

< /p >


< p > < strong > which products belong to BPR biocide treatment products (TA) < /strong > /p >


< p > according to the definition and the applicable conditions of TA in the BPR regulations, TA will cover many industries and products, including electronic appliances, textiles, leather products, rubber, plastic products, furniture and household products, as well as common objects such as paint, paint or emulsion products.

< /p >


< p > BPR requirements for biological killer products (TA) < /p >


All active substances in biological biocides handled by < p > 1. must be included in the list specified in < a href= "//www.sjfzxm.com/news/index_c.asp" > BPR < /a > ninth (and conforms to the relevant product types and conditions of use) or in BPR appendix I (and comply with all the conditions and restrictions).

Otherwise, the TA should not be put on the market.

< /p >


< p > 2. when TA meets the following circumstances, the manufacturer and importer need to label the treated items.

< /p >

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