About Jessica

Jessica focuses on European law and the regulation of medicinal products and medical devices, including in vitro diagnostic medical devices. She 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.

View full bio

Experience

View more

Admissions and credentials

  • Brussels (A List)

This content is provided for general informational purposes only, and your access or use of the content does not create an attorney-client relationship between you or your organization and Cooley LLP, Cooley (UK) LLP, or any other affiliated practice or entity (collectively referred to as "Cooley"). By accessing this content, you agree that the information provided does not constitute legal or other professional advice. This content is not a substitute for obtaining legal advice from a qualified attorney licensed in your jurisdiction, and you should not act or refrain from acting based on this content. This content may be changed without notice. It is not guaranteed to be complete, correct or up to date, and it may not reflect the most current legal developments. Prior results do not guarantee a similar outcome. Do not send any confidential information to Cooley, as we do not have any duty to keep any information you provide to us confidential. When advising companies, our attorney-client relationship is with the company, not with any individual. This content may have been generated with the assistance of artificial intelligence (Al) in accordance with our Al Principles, may be considered Attorney Advertising and is subject to our legal notices.