Tag: EU Legislation
New EU liability rules proposed for artificial intelligence
Rod Freeman, Claire Temple, Jamie Humphreys and Tracey Bischofberger
European Commission publishes new liability rules to simplify claims for damage caused by AI-systems
Radical Reform of EU Product Liability Laws: Long-awaited Proposals Published
Rod Freeman, Claire Temple, Ed Turtle and Tracey Bischofberger
European Commission publishes long-awaited proposals for reforming EU product liability rules
Productwise Bitesize: The Construction Products Regulation
Jamie Humphreys and Julia Maskell
Productwise Bitesize brings you a short introduction to the Construction Products Regulation (CPR), which sets out the requirements for construction products in the EU.
European Commission proposes to up-classify certain beauty equipment falling within EU Medical Devices Regulation
Elizabeth Anne Wright , Emma Bichet and Alexander Wenzel
Read our summary on the proposed up-classification of certain products falling within EU Medical Devices Regulation.
Productwise Bitesize: In Vitro Diagnostic Medical Devices Regulation
Alexander Wenzel and Jessica Koffel
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.
Productwise Bitesize: Low Voltage Directive
Jamie Humphreys and Harriet Jones
Productwise Bitesize brings you a short introduction to the Low Voltage Directive, a key piece of EU legislation setting out health and safety standards for electrical equipment.
Rapid-Fire Update on International Developments in Products Law: Webinar Recording
Access a recording of the Cooley team’s rapid-fire overview of important changes in EU and US products law.
WEBCAST: Rapid-Fire Update on International Developments in Products Law
Tune in for a 30-minute rapid-fire webinar on recent developments in product regulation and product liability in the EU and US.
Productwise Bitesize: Medical Devices Regulation
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 […]
Don’t let this opportunity go to waste – WFD Consultation now open
Read on to learn more about the proposed revision of EU waste legislation.