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Valerie Mei is an associate in the Frankfurt office and member of the firm's Food, Drug and Device Practice Group and also a member of our Global Compliance practice. She advises clients on a broad range of regulatory and compliance matters, including medical device and pharma regulation and healthcare compliance issues. Her practice also includes data protection and general contractual matters.

  • COVID-19 related matters (Clinical trials, special authorizations of medical devices).
  • Advised a large medical device manufacturer on MDR implementation issues from a regulatory perspective.
  • Advised medical device manufacturer on requirements for conformity assessments and conformity declarations.
  • Advised pharmaceutical manufacturers on regulatory issues related to pharmacovigilance, medical information, and GMP.
  • Compliance review of agreements between pharma companies and healthcare professionals and healthcare organizations.
  • Review and drafting of clinical trial agreements.
  • Classification of medical software and medical apps.

Previous Experience

  • During her legal clerkship, Valerie Mei worked inter alia at a German civil court, in the legal department of a large international company and in a municipal authority in Germany.