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THOUGHT LEADERSHIP
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March 03, 2021
EU-UK Trade and Cooperation Agreement: Implications for Life Sciences Companies
The agreement provides guidance across several areas for the life sciences sector, though gaps remain.
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February 19, 2021
Life Sciences Law Review - 9th Edition, France Chapter
Latham lawyers Eveline Van Keymeulen and Jeanne Fabre discuss essential rules on medicines and medical devices under the French regulatory regime, for the Life Sciences Law Review.
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December 17, 2020
Antitrust Enforcement in Health Care: A Risky and Evolving Landscape
A cross-country team of litigators examines the US Department of Justice trends in antitrust enforcement in the last 18 months for In Vivo, the premiere resource for life sciences business strategy.
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September 30, 2020
Securities Litigation Trends During Covid-19
In an article for Bloomberg Law, partners Blair Connelly and Colleen Smith and associate Cindy Guan, explore patterns emerging in securities litigation in the age of the pandemic.
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September 25, 2020
UK Issues New Guidance for Medical Device Regulation After Brexit
The MHRA offers new guidance on how medical devices will be regulated in the UK from 1 January 2021.
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September 21, 2020
Healthcare AI Deals a Tonic for PE Investors
Healthcare artificial intelligence is a promising sector for PE investors that requires careful navigation, particularly given divergent regulatory approaches.
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July 07, 2020
COVID-19: Managing Worker Health & Safety
Federal and state guidelines for employers that are reopening their business premises in the US.
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May 28, 2020
Rise in Securities Class Action Filings in Life Sciences Sector
Last year proved to be another record period for securities class actions, with a 13% increase in cases filed compared with 2018, and a 24% increase in claims brought against life sciences companies compared with 2018, write partners Michele Johnson and Colleen Smith in In Vivo.
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April 08, 2020
COVID-19: DHSC and MHRA Pave the Way for Increased Ventilator Production
UK companies interested in producing ventilators and other critical equipment may benefit from regulatory exemptions and use government product specifications.
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April 07, 2020
New EU Medical Devices Regulation to Be Postponed Until 2021
European Commission proposes one-year postponement in light of the COVID-19 crisis.
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