Vici delivers end-to-end drug development solutions for emerging 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.
cGMP-certified
GLP-certified
DEA license – Schedule I-V