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MedTech Summit

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Hybrid Event, 20 - 24 June 2022
In-Person: Clayton Hotel Burlington Road, Dublin, IrelandDigital Experience: One track will be live-streamed each day in BST time zone, with on-demand recording access for all other tracks made available from the afternoon of the following day. Learn more on the Digital Experience page.

Jessica Koffel
Associate at Cooley LLP

Profile

Jessica is an associate with the Cooley Brussels Life Sciences Team. She focuses on European law and the regulation of medicinal products and medical devices, including in vitro diagnostic medical devices. Jessica helps guide life sciences companies through the regulatory processes and technical requirements governing the approval and marketing of their products – from classification, clinical trials and audits to promotion and marketing. Jessica provides strategic advice from the early development stages to placing on the market and post-marketing activities. She also assists clients in their interactions with regulatory authorities, notified bodies and business partners.

Prior to joining Cooley, Jessica worked as an associate in leading international law firms, where she focused on the EU regulation of life sciences products and chemicals.

Agenda Sessions

  • Addressing the Legal Requirements for Medical Device Clinical Investigations

    14:30