Productwise Bitesize brings you a short introduction to the Construction Products Regulation (CPR), which sets out the requirements for construction products in the EU.
Productwise Bitesize brings you a short introduction to the In Vitro Diagnostic Medical Devices Regulation. Since 26 May 2022, this regulation has been applicable to IVDs, and their manufacturers, importers, distributors and online sales at a distance.
Cooley’s Productwise Bitesize brings you a short overview of the EU Medical Devices Regulation. What is it called? The Medical Devices Regulation (MDR Regulation (EU) 2017/745) governs the placing on the market in the European Economic Area (EEA) of medical devices and its accessories as well as clinical investigations taking […]
Productwise Bitesize brings you a short introduction to the Delegated Act to the Radio Equipment Directive on cybersecurity, which aims to increase the level of cybersecurity of wireless devices placed on the EU market.
CE marking refers to the obligation on manufacturers to affix the letters “CE” to certain products traded in the European Economic Area (EEA). It serves as a declaration that the product is in conformity with applicable rules and meets certain health, safety and environmental requirements.
Cooley’s Productwise Bitesize brings you a short introduction to the update to the “Blue Guide” on the Implementation of EU product rules.