All posts by Cooley

Productwise Bitesize: the General Product Safety Directive

Jamie Humphreys and Julia Maskell

Cooley’s Productwise Bitesize brings you a short introduction to the “General Product Safety Directive”.

Productwise Bitesize: New Deal for Consumers

Jamie Humphreys, Edward Turtle and Julia Maskell

Cooley’s Productwise Bitesize brings you a short introduction to the “New Deal for Consumers”.

UK’s medicines and medical devices regulator to tackle Brexit, technological advancements and regulatory challenges (including from COVID-19) in 2020 and 2021

Sarah-Jane Dobson and Amal Ali

The MHRA has established five strategic goals for 2020-21 that will impact all those operating in the UK medicines and medical devices industries

WEBCAST: Moving to a Circular Economy

Cooley’s international products law team are pleased to announce the fifth event in its webinar series, together with experts from Compliance & Risks and Ramboll. As an area of major regulatory and business change for product manufacturers, suppliers and other stakeholders, we anticipate the impact of the move towards the […]

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 […]

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.