The Arcinova Advantage: Built for Clinical Development Success
Integrated formulation development, GMP manufacturing and CMC regulatory expertise to help advance drug product programmes into first-in-human studies.
Reduce Development Risk
40+ years of formulation development and manufacturing expertise across oral, parenteral and radiolabelled drug products.
Enable Challenging Molecules
Integrated support for poorly soluble molecules through tailored formulation and bioavailability-enhancing strategies.
Accelerate Clinical Studies
Flexible GMP manufacturing capabilities supporting sterile injectables, FIH and human ADME studies.
Manufacture with Confidence
Submission-ready CMC documentation supported by integrated analytical, microbiological and regulatory expertise.
From simple capsule formulations to complex sterile injectables
Arcinova provides phase-appropriate drug product solutions tailored to the needs of your molecule and development programme, ranging from simple capsule formulations to complex sterile injectables and bioavailability-enhancing technologies. Our scientists combine formulation, analytical, manufacturing and regulatory expertise to develop robust drug products that support rapid progression to the clinic.
With over 40 years of experience, we tailor each solution to your molecule's physicochemical and biopharmaceutic profile, route of administration and stage of development, helping accelerate programmes while maintaining scalability and regulatory readiness.
Oral, Parenteral & Radiolabelled Drug Products
Poorly Soluble Molecule Expertise
FIH & Human ADME Support
Submission-Ready CMC Packages
An integrated approach to drug product development
Successful drug products require more than formulation expertise alone. Arcinova brings together drug product development, analytical science, GMP manufacturing and CMC regulatory support within a single programme team.
By integrating these disciplines from the outset, we help reduce handovers, minimise development risk, support regulatory readiness and accelerate progression to clinical milestones including FIH and human ADME studies.
- Formulation Development
- Analytical Sciences
- GMP Manufacturing
- CMC Regulatory Support
40+ Years
Formulation development & manufacturing experience
48,000 ft²
Purpose-built drug product facility
1,500+
Formulations developed
Experienced Teams
Formulation, manufacturing and CMC specialists