Your CDMO Partner
from Concept to Clinic
Delivering drug development solutions for emerging pharma.
CDMO SERVICES
Formulation Development
Unmatched formulation development expertise to accelerate your drug development program.
Clinical Supply Chain
We focus on quality and speed to ensure your clinical studies are completed on time.
Regulatory Services
Providing you with 505(b)(2) and ANDA regulatory strategy and filing services.
What We Do
We are experts at formulation development, analytical method development, manufacturing process development and tech transfer, CRO management for BE studies, CMC regulatory documentation, and regulatory filings.
About
Vici Health Sciences
Vici delivers end-to-end drug development solutions for small pharma. We provide formulation development, analytical method validation and testing, cGMP clinical supplies manufacturing, FDA regulatory services, and CMC R&D consulting services. We are experts in NCE molecule development, NDA 505(b)(2), and ANDA development programs. Our experienced formulation scientists and chemists solve problems through innovation, speed, and flexibility offering excellent value for companies needing better R&D outcomes. Vici operates a pharmaceutical R&D center of excellence in Maryland, USA.
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