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.
Formulating the future takes more than good intentions - it takes a system that works. Our model simplifies your path to market by connecting the dots between sourcing, compliance, and manufacturing.
End-to-end support for global filings (DMFs, CEPs, CTDs) to accelerate approvals.
Production through WHO, USFDA, and EU-approved facilities - without capital investment.
A connected, transparent pharma supply chain that drives predictability and speed.
Behind every partnership is a team built for scale, speed, and trust. Our specialists combine scientific depth with strategic execution - solving complex challenges and turning vision into delivery.
We serve pharmaceutical partners across 55+ countries
offering regulatory guidance, manufacturing access, and market integration wherever innovation is needed most.
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?
Choose HRV Pharma as your global pharma partner. From sourcing to delivery, we bring together innovation, regulatory precision, and a partner-first mindset - all in one agile platform.
