We go beyond traditional CDMO roles - seamlessly uniting top-tier cGMP manufacturers under one virtual platform, ensuring compliance and fast-tracking your global reach.
Our agile, asset-light model blends manufacturing excellence with regulatory know-how to bring medicines to patients worldwide swiftly and reliably.
In Pharma, Access is Everything.
Three core capabilities that accelerate your pharmaceutical market expansion through our proven asset-light model and regulatory expertise.
We handle your complex global regulatory filings (DMFs, CEPs, CTDs) and handle the compliance process for 5x faster market entry.
Our curated network of USFDA, WHO, and EMA-approved facilities delivers quality production without capital investment.
From sourcing to delivery, we connect every dot. Experience total supply chain visibility and the power of predictable outcomes.
Our lean, expert team combines deep pharmaceutical knowledge with innovative thinking. We move fast without missing critical details.
Serving pharmaceutical needs across key global markets
FDA regulatory expertise
FDA Experts
EMA compliance & CEPs
EU Regulatory Access
Award-winning expansion
Award Winner
Government partnerships
Gov Partnerships
Emerging market solutions
Emerging MarketsWhy Choose HRV as Your Pharmaceutical Partner?
We bring together quality materials, expert manufacturing, precise regulatory work, and smart logistics to deliver life-saving medicines to patients everywhere.
