Business Details
Your Partner for Integrated Drug Development Solutions
Quotient Sciences is a global leader in drug development and manufacturing acceleration, dedicated to transforming innovative pharmaceutical ideas into successful therapies. Our integrated approach combines clinical research, real-time manufacturing, and scientific expertise to streamline the path from candidate selection to commercial supply. With over three decades of experience, we serve biotech startups and Fortune 100 pharmaceutical companies, offering tailored solutions for complex drug development challenges. Our science-led methodology prioritizes speed and efficiency, ensuring therapies reach patients faster. Headquartered in the United States with international operations, we maintain strategic partnerships and global infrastructure to support clients worldwide.Our commitment to innovation is reflected in our patented Translational Pharmaceutics platform, which reduces development timelines by integrating clinical and manufacturing processes. Recognized for excellence through multiple CDMO Leadership Awards, we continuously invest in cutting-edge technologies and sustainable practices. Our team of experts collaborates closely with clients to navigate regulatory milestones and optimize drug formulations. By maintaining transparency and ethical standards, we build long-term trust with partners and stakeholders. Our mission remains focused on accelerating life-saving treatments while maintaining the highest quality and compliance benchmarks.
Services
Drug Product Manufacturing
Integrated Drug Development
Phase I Clinical Studies
Pediatric Formulation Development
Commercial Drug Manufacturing
Formulation Development
First-in-Human Clinical Trials
Clinical Pharmacology
Drug Product Optimization
Highlights and features
- We offer 30+ years of experience in pharmaceutical drug development
- Our integrated CRDMO model streamlines clinical and manufacturing processes
- We provide science-led solutions for complex formulation challenges
- Our global presence supports clients across 30+ countries
- We maintain partnerships with leading pharmaceutical companies
Services
Integrated Drug Development
Our integrated approach combines clinical research and manufacturing to accelerate drug development timelines. By eliminating traditional handoffs between phases, we reduce time-to-market while maintaining regulatory compliance. This methodology supports both small and large molecule development across therapeutic areas.
First-in-Human Clinical Trials
We conduct Phase I clinical studies with specialized pediatric formulation capabilities. Our facilities enable rapid transition from preclinical to human testing, supported by real-time manufacturing adjustments. This approach improves decision-making efficiency during early development stages.
Commercial Drug Manufacturing
Our cGMP manufacturing services support commercial-scale production with flexible capacity. We maintain global facilities to meet regional regulatory requirements while ensuring consistent product quality. This service includes both solid and liquid dosage form production.
Pediatric Formulation Development
We develop age-appropriate formulations for pediatric indications using innovative taste-masking and delivery technologies. Our platform addresses bioavailability challenges while ensuring compliance with regulatory guidelines for children's medicines.
Translational Pharmaceutics
This proprietary platform integrates drug development activities across discovery, clinical, and manufacturing functions. By enabling real-time data sharing between disciplines, we achieve faster optimization cycles and reduce development risks for complex molecules.
Questions
What makes Quotient Sciences different from other CDMOs?
Our integrated model combines clinical development and manufacturing under one organization, eliminating traditional handoffs to accelerate timelines by up to 18 months.
Do you work with both small and large pharmaceutical companies?
Yes, we serve emerging biotechs through Fortune 100 pharmaceutical companies, providing tailored solutions for projects of all sizes and complexities.
What therapeutic areas do you specialize in?
We have expertise across oncology, CNS disorders, metabolic diseases, and rare conditions, with specialized capabilities in pediatric formulations.
How do you ensure regulatory compliance?
Our global quality system maintains cGMP compliance across all facilities, with experienced regulatory affairs teams supporting submissions in major markets.
Can you handle complex molecule development?
Yes, our Translational Pharmaceutics platform is specifically designed to address challenges with poorly soluble, unstable, or difficult-to-formulate compounds.
