We specialize in optimizing bioavailability, stability, and delivery methods across many dosage forms. Through robust QA oversight—whether addressing complex solubility challenges or fine-tuning release profiles—we ensure each formulation is designed for maximum efficacy and safety. Our end-to-end approach integrates seamlessly with analytical testing and manufacturing to deliver reliable, patient-focused solutions. Explore our features to see how we transform demanding formulation challenges into successful outcomes.
Benuvia’s formulation expertise was a game-changer for our project. Their team’s ability to tailor solutions and optimize stability gave us a competitive edge. The seamless integration with their manufacturing services saved us time and ensured our product met the highest quality standards.
Specialty Pharmaceutical Client
Director of Product Development
Our formulation development services deliver results that align with your goals and regulatory requirements.
Explore our formulation development case studies to see how Benuvia has transformed challenges into innovative solutions. Discover the expertise, technology, and precision that drive our success and yours.
Dr. Muthiah Chinnasamy, Vice President of API and Formulation R&D, has over two decades of experience in pharmaceutical R&D and manufacturing. His expertise spans API process development, regulatory compliance, and managing CDMO operations across the globe.
With leadership roles at organizations like Cambrex and Bachem, Muthiah has developed FDA-approved drugs, optimized manufacturing processes, and prepared over 300 business proposals. A Ph.D. in synthetic organic chemistry with international postdoctoral experience, he brings a global perspective to solving complex challenges.
Muthiah is passionate about advancing pharmaceutical innovation and is eager to share his insights, answer your questions, and discuss how Benuvia can support your API and formulation development needs.
"*" indicates required fields
Notifications