Category: Ongoing Compliance
See EU later – the UK government has issued guidance on placing manufactured goods on the market in post-Brexit Great Britain and using the UKCA mark from 1 January 2021
Tracey Bischofberger, Rod Freeman and Claire Temple
Here’s our snap review of the guidance issued today…
Productwise 3-2-1
Tracey Bischofberger, Matt Howsare and Claire Temple
Productwise 3-2-1, our monthly bite-sized digest of the current key issues in products law.
Representative actions and insurance: some looming traps for product manufacturers
Introduction As reported in our earlier blog, a compromise has recently been reached in respect of the content of a new EU Directive on consumer collective redress (the Directive), with the final directive likely to come into force by the end of the year and member states to transpose it […]
Productwise 3-2-1
Tracey Bischofberger, Matt Howsare and Claire Temple
Introducing Productwise 3-2-1, our monthly bite-sized digest of the current key issues in products law.
General Product Safety Directive Consultation: Commission Checks its Safety Net for Holes
Jamie Humphreys and Edward Turtle
The European Commission is holding a consultation on proposed amendments to the EU’s General Product Safety Directive.
COVID-19: Weekly Life Sciences Digest – International Collaboration and Adjusted Exports/Import Rules
Sarah-Jane Dobson, Edward Turtle and Alicia Johnson-Cole
With COVID-19 heralding unprecedented changes in the sector, our life sciences products experts provide a weekly summary of key international developments to keep you up to date.
Flexibility for our furry friends
Sarah-Jane Dobson and Olivia Flasch
EU regulators have taken steps to address supply chain disruption and increased demand in veterinary medicines caused by the COVID-19 pandemic.
WEBCAST: EU and AI – Navigating the European Approach
Cooley’s international products law team are pleased to announce the fourth event in its webinar series. This webinar will look at the European Union’s approach to Artificial Intelligence including the impact of the European Commission’s White Paper on Artificial Intelligence. The team will be joined by members of Cooley’s Technology […]
UK-specific guidance for the application and management of clinical trials in the context of COVID-19
Sarah-Jane Dobson and Amal Ali
The UK’s MHRA has stated it will be particularly flexible and pragmatic in authorising clinical trials connected to COVID-19, referring to its previous track record of having acted swiftly in past public health crises
WEBCAST: Products & Consumer Rights: Global Hot Topics
Cooley’s international products law team is pleased to announce the third event in its webcast series looking at the latest consumer rights issues product manufacturers, suppliers and other stakeholders are facing in the rapidly changing global environment. This time we will be joined by Wendy Hederman, a partner at leading Irish law […]
