Share:

Elizabeth Anne Wright is a Partner with Cooley and specializes in European Union law and regulation of pharmaceuticals and medical devices. She advises clients and publishes extensively on digital health issues, such as their implications for CE marking obligations for medical devices, and related obligations for life sciences companies. She has been practicing in the life sciences sector for over 35 years in private practice and international institutions. She helps clients navigate the process and regulations to place and keep their products on the European Union market through strategic advice, advocacy before institutions and agencies, and litigation before EU courts.

Share: