Our Experience. Your Success.

Greenleaf’s decades of hands-on experience in the regulatory space is unmatched. The firm’s team of experts equips clients with a trusted partner when navigating the complexities of developing medical products for the U.S. market and manufacturing them to FDA quality standards.

GLH FAQ

  • Greenleaf Health is a full-service FDA regulatory consulting firm guiding companies through the changing FDA landscape.
  • Greenleaf is headquartered in Washington, D.C., with offices in Chicago and Palo Alto.
  • Greenleaf provides global services to companies, trade associations, and other stakeholders regulated by the FDA.
  • Greenleaf’s team is comprised of experts with a combined total of more than 250 years of FDA experience.
  • The firm‘s team of experts includes former leaders and regulatory professionals from the FDA, Capitol Hill, top global pharmaceutical and medical device companies, leading law firms, and the top U.S. biotechnology trade organization.
  • Greenleaf professionals work as teams specializing in product quality, manufacturing, and compliance; medical devices and combination products; and drug and biological products.