The EN 18031-series of standards will soon be harmonised and then provide a presumption of conformity with the essential requirements in Article 3(3) of the RED 2014/53/EU and Delegated Regulation (EU) 2022/30 on cybersecurity.
The PFHxA restriction enters into force on 10 October 2024, taking effect after transitional periods between 18 months and 5 years.
The main driver of deforestation and forest degradation is the expansion of agricultural land, which is linked to the production of seven commodities: cattle, cocoa, coffee, oil palm, rubber, soya, and wood; and some of their derived products, such as leather or furniture.
Overall, around 145,000 tonnes of microplastics are estimated to be used in the EU each year. And 42,000 tonnes of these microplastics end up in the environment from products intentionally containing them. The largest contribution with up to 16,000 tonnes is made by granules from artificial turf pitches.
There are many directives and regulations that address product compliance. Still it is practically impossible to cover all risks for all consumer products. The solution is a broad-based legislation to fill possible gaps and to complement existing and future legislation.
The importance of the document. Manufacturers have to make sure that their products comply with all applicable legislation. Once they have done this, they create and sign a document called an EU Declaration of Conformity (DoC) to underwrite that their product satisfies all applicable EU legislation.
In various pieces of legislation you will find the passage: “the marking shall be affixed visibly, legibly and indelibly”. It makes perfect sense that markings remain present and usable throughout the entire lifecycle of the product. But how can you show in a practical way that all three criteria are met?
Since Brexit, the UK CPR has superseded the regulation (EU) No. 305/2011 in England, Scotland and Wales. The European CPR will remain to apply in Northern Ireland. The EU CPR is subject to CE-marking and the UK CPR is subject to UKCA marking.
The impact of Brexit on product compliance is big. The basis for almost all United Kingdom (UK) product legislation was based on EU-law.
The EU Single Market consists of the Member States of the EU. The objective is that within the EU Single Market, products, capital, services and people can flow freely from one Member State to another Member State.
Biocides are chemicals intended to kill or destroy living (micro)organisms. Preservatives are chemicals used in textiles to prevent the growth of microorganisms. Both biocides and preservatives are biocidal substances which are regulated due to major health and environmental concerns.
Wireless products require radio frequencies to work. The allocation of frequencies is done by each Member State in their regional frequency plans or registers. Once frequencies are allocated for a certain use, it is difficult to allocate these frequencies for other uses as well without causing interference with
The letters ‘CE’ appear on many products in the EU. CE stands for the French ‘Conformité Européenne’, which translates to ‘European Compliance’. Manufacturers of products with the CE-marking declare that the products meet high safety, health and environmental protection requirements in response to EU legislation.
The Construction Products Regulation (CPR) requires mandatory CE marking for construction products covered by a harmonised standard. Compliant construction products with CE marking can be placed legally on the market in any Member State.
The first directive on Restriction of Hazardous Substances (RoHS) in electrical & electronic equipment (EEE) was published back in 2003. On 3 January 2013 the second directive (RoHS2) came into force: Directive 2011/65/EU.