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Africa Zero Liquid Discharge System Market Research Report By Key Players Analysis Till 2033

Posted by Latest Market Trends on March 28, 2024 at 12:08pm 0 Comments

The Africa zero liquid discharge system market is poised for significant advancement, with a projected valuation surpassing US$ 53.1 million by 2033. This growth trajectory, characterized by a robust Compound Annual Growth Rate (CAGR) of 5.6% from 2023 to 2033, is underpinned by several factors, including the adoption of cutting-edge wastewater treatment processes and the notable efficiency enhancements offered by ZLD systems compared to conventional Effluent Treatment Plant (ETP)… Continue

What’s New in The European Authorized Representative Regulation?

What’s New in The European Authorized Representative Regulation?

This new regulation will affect all companies that sell CE-marked products manufactured outside the European Union

As the Brexit transition period is over, this includes UK-made products, but also e-commerce and e-business companies like Amazon. Therefore, resellers of CE-marked products should make sure that their suppliers have made the necessary arrangements for the designated agent.

As of July 16, 2021, the new regulation 2019/1020 / EU (Market surveillance and product compliance) will come into force. After this date, CE-marked products cannot be sold in Europe without an authorized representative based in the EU.

Please note that medical devices, cableway facilities, civilian explosives, kettles, and elevators are not affected by this new standard.

Who to choose?

An authorized representative in the EU can be:

  • The manufacturer or brand
  • The importer
  • An authorized representative designated by the manufacturer

This person must be established in the European Union.

What are your obligations?

Before July 16, 2021, the affected companies must ensure that their CE-marked products continue to meet quality and safety standards and that they carry the contact details of the authorized representative. 

This labeling can be done on the product, on its packaging, or in an accompanying document.

They will have to collect the declaration of conformity and ensure that additional documents are available upon request from the authorities.

In certain cases, you will also have to alert the authorities to the risks posed by the products, cooperate with the authorities in market surveillance, and ensure that the manufacturer takes the necessary steps to remedy the non-conformity of the product.

After the deadline, it will be illegal to sell CE-marked products in the EU without a designated representative established in the area and without a proper label.

CE marking: a European quality guarantee

The CE marking has been created within the framework of European technical harmonization legislation. By affixing the CE marking to its products, a manufacturer declares that its products comply with European legal standards and can be sold in the European Union

You take responsibility for complying with all European health, safety, performance, and environmental protection requirements that apply to your product

“CE” stands for “European Conformity“. Therefore, it is not a certification mark or an indication of the geographical origin of the product

The CE marking must be visible, legible, and indelible. There are many categories of products that can carry the CE marking: they can be machines, toys, or televisions.

The absence of marking or “false marking” can be sanctioned through administrative and criminal procedures.

Do you want to know more about European regulations? Visit www.i3cglobal.com

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