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.
Homologation is the process by which a product or vehicle is certified as compliant with the technical and safety standards required for its use in a particular region or country.
Consumers or users shall be provided with information to use products as intended. Information about the risks inherent in a product is essential for safe use; especially where the risks are not immediately obvious.
Consumers or users shall be provided with information to use products as intended. Information about the risks inherent in a product is essential for safe use; especially where the risks are not immediately obvious.
Chances are that your product contains PFAS and PFCA! Restrictions are already in place. Some additional restrictions will come into effect early next year. PFAS are used in a wide variety of consumer products because of their unique chemical and physical properties.
Chances are that your product contains PFAS and PFCA! Restrictions are already in place. Some additional restrictions will come into effect early next year. PFAS are used in a wide variety of consumer products because of their unique chemical and physical properties.
Due Diligence has been, up to now, largely a matter of self regulation*. Some EU Member States already have Due Diligence legislation, but the problem is only that this legislation is either too sector-specific or only covers certain aspects of the Due Diligence.
Homologation is the process by which a product or vehicle is certified as compliant with the technical and safety standards required for its use in a particular region or country.
UKCA marking is a similar provision as the CE marking, however applicable for UK laws and the UK market.
Consumers or users shall be provided with information to use products as intended. Information about the risks inherent in a product is essential for safe use; especially where the risks are not immediately obvious.
There will be a new regulation on the safety of toys. On July 28, the European Commission published a proposal. This proposal will be voted on in rounds by the European Parliament and the Council and is expected to be largely approved in the foreseeable future.
The obvious objective of conformity assessment is to demonstrate that all products conform to relevant legislation. The manufacturer always remains responsible for the execution of conformity assessment, even if design, tests, documentation or production is subcontracted. The manufacturer also remains responsible
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.