Lucas Michel

Lucas is an associate in the Life Sciences practice.

He advises clients across a wide range of regulatory, compliance and procedural issues in the food, pharma, and medical devices sectors, with a focus on EU and Belgian regulatory advice.

Lucas also assists clients on public procurement matters, ESG queries, and represents clients in Belgian and EU courts.

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EU Health Emergency Mechanisms: Impact on Medical Devices

By Sarah Cowlishaw, Lucas Michel & Zoé Bertrand on March 26, 2024

Posted in COVID19, European Union, Food & Drug Regulatory, Life Sciences, Medical Devices

The European Union has adopted various new rules for emergency situations relating to public health. These new measures build on the experience gained from the COVID-19 pandemic and give new powers to the European Commission, in close cooperation with the Member States.

The new rules create a complex public health…

Single Market Emergency Instrument: Potential Impact on Medical Devices

By Sarah Cowlishaw & Lucas Michel on January 16, 2024

Posted in COVID19, European Union, Food & Drug Regulatory, Life Sciences, Medical Devices, Medical Devices, Patents

The European Parliament and Council are currently negotiating the wording of a new Regulation establishing a Single Market emergency instrument (“SMEI”). This new measure builds on the experience gained from the COVID-19 crisis and gives new powers to the Commission, in close cooperation with the Member States. This blog briefly…

Inside EU Life Sciences

Lucas Michel

EU Health Emergency Mechanisms: Impact on Medical Devices

Single Market Emergency Instrument: Potential Impact on Medical Devices

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