Morrison & Foerster’s full-service FDA Regulatory Practice advises clients in the life sciences industry, helping them navigate complex regulatory, compliance, health care system, and marketplace issues. With a strategic and comprehensive life-cycle approach, our experienced lawyers counsel domestic and international clients, from pre-product launch to post-market representation. We counsel clients in the medical device, pharmaceutical, food and dietary supplement, biotechnology, healthcare technology, and cosmetic industries, ensuring that they are FDA compliant as well as optimally positioned for maximum coverage and reimbursement, entry into new global markets, and further research and development.
Our clients include:
Consistent with MoFo's collaborative approach, we work seamlessly with other lawyers across the firm to meet our clients’ comprehensive needs regarding FDA regulations, compliance, enforcement, policy, and strategic counsel, as well as with our Consumer Products and Global Privacy + Data Security teams on HIPAA, connected health, and clinical trial compliance matters, among others. This integrative approach provides our clients with the highest quality counsel for developing cutting-edge solutions that ensure product compliance and maximal market potential.
Complete Product Life Cycle Counsel
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