Hogan Lovells International LLP

Medical Device & Technology

Senior Associate

As a member of Hogan Lovells' Global Regulatory Life Sciences team, Cláudia Mendes Pinto advises clients in the pharmaceutical, medical devices and biotechnology sectors on a wide range of regulatory and commercial law matters. throughout their products’ life-cycle, from early development stages to certification/authorisation, and post-market issues. This includes product qualification and classification, determination of regulatory pathways, authorisation and conduct of clinical studies, CE marking of medical devices and IVDs, GxP matters, interactions with regulatory authorities and notified bodies, pricing and reimbursement and post-market activities. Cláudia also frequently assists life sciences clients with a variety of agreements and she has experience in internal investigations, regulatory due diligence for mergers and acquisitions, coordination of multijurisdictional projects, as well as litigation in state and arbitral courts.

English, French, Portuguese