Claire Temple, Emma Bichet and Selma Abdel-Qader
Productwise guides you through the European Commission’s new initiative on cybersecurity requirements.
Elizabeth Anne Wright and Alexander Wenzel
Cybersecurity requirements established in the NIS 2 Directive apply to medical device manufacturers
Rod Freeman, Jamie Humphreys and Tracey Bischofberger
OPSS publishes PRISM – a new approach to risk assessment in the UK
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.
Tune in for a 30-minute rapid-fire webinar on recent developments in product regulation and product liability in the EU and US.
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 […]
Edward Turtle and Tracey Bischofberger
The hotly-anticipated revision of the European Commission’s Blue Guide has been published. Here’s our take on why this matters to anyone involved in the manufacture, import or sale of products in the EU.
Edward Turtle , Jamie Humphreys, Corinne Robinson and Jack Eastwood
UK publishes new report on the impact of Artificial Intelligence on product safety and liability.
Tracey Bischofberger, Matt Howsare, Shawn N. Skolky and Claire Temple
Productwise 3-2-1, our monthly bite-sized digest of the current key issues in products law.