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.
UK Government Announces Extension to Key UKCA Grace Periods
The UK government has announced it intends to extend the key UKCA and GB importer labelling grace periods, to assist businesses in complying with the post-brexit requirements for products sold in Great Britain.
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 […]
The New Blue: EU Updates Key “Blue Guide” to Products Laws
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.
Productwise Bitesize: New EU rules on cybersecurity adopted under the Radio Equipment Directive
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.
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.