About Us
MedoPharm began as a two‑person regulatory consultancy in 2000. Twenty‑five years later, we manage more than 600 SKUs under GDP conditions, hold direct import licences in Paraguay, and guide Asian manufacturers through every ANVISA and MERCOSUR requirement—from stability protocol to first commercial lot. Our independence ensures one point of accountability from factory gate to hospital shelf.
Mission, Vision & Core Values
Mission
To be the trusted conduit for pharmaceutical innovators, delivering turnkey licensing, technology transfer and GMP certification solutions that empower success in MERCOSUR and Asia.
Vision
To redefine cross-continental pharmaceutical excellence—building seamless bridges between Asian API hubs and South American markets, and enabling faster access to safe, effective medicines for patients worldwide.
Core Values
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Client-Centric Partnership
Act as an extension of our clients’ teams—anticipating needs, customizing solutions, and sharing risks.
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Collaborative Innovation
Foster open, transparent alliances with manufacturers, CROs and authorities to drive continuous improvement.
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Relentless Agility
Adapt swiftly to evolving regulations, technologies and market dynamics to keep our clients ahead.
