
Products treated with biocides, and biocidal products imported or manufactured in the European Union must adhere to the requirements of the Biocidal Products Regulation. In some situations, even making biocidal claims about the product may trigger the requirements of the regulation, which include labelling, documentation and testing.
The Biocidal Products Regulation can therefore be applicable to, for example, socks designed to prevent odour. Another scenario could be underwear with claimed anti-bacterial properties.
The guide is split into two parts. The first half elaborates on the regulation’s requirements for treated products, such as garments. The second half focuses on requirements affecting biocidal products.
Continue reading Biocidal Products Regulation: An Essential Guide











The Medical Devices Regulation sets requirements according to device class. More specifically, medical devices are defined as class I, IIa, IIb, or III. In turn, this determines certain requirements, and which conformity assessment procedure the manufacturer must follow.