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The Trials and Tribulations of the Medical Devices and IVD Regulations, European Pharmaceutical Review

August 25, 2020

Morgan Lewis consultant Paul Ranson authored an article for European Pharmaceutical Review in which he explores the reasons behind the introduction of the EU Medical Device and In Vitro Diagnostic Devices Regulations. Paul examines issues with the regulations, including the impact of the coronavirus (COVID-19), which ultimately convinced the Commission that another year of preparation would be needed to fully apply them.

Read the full article on European Pharmaceutical Review >>