Drug Product Services

Integrated formulation, manufacturing and CMC expertise to help you reach the clinic faster.

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.

 

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 
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Drug product and analytical chemists
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40+ year formulation development & manufacturing experience

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Purpose built 48,000ft2 drug product facility

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Experienced  formulation, development and manufacturing teams

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Over 1,500 formulations developed

Integrated regulatory expertise, built into your DS and DP development.
Partner with us for consistent, accurate CMC submissions and rapid issue resolution.

The Arcinova Advantage:

  • 40+ years' formulation development and manufacturing experience
  • Expertise across oral, parenteral and radiolabelled drug products
     
  • Integrated support for poorly soluble molecules
  • GMP aseptic manufacturing for sterile injectables
  • Analytical and microbiological expertise built into development programmes
  • Submission-ready CMC regulatory support
  • Proven support for FIH and human ADME studies 
     

From formulation concept to clinical supply

Whether you require a simple early-phase formulation, sterile injectable manufacture, support for a poorly soluble molecule, or integrated CMC regulatory expertise, Arcinova provides the scientific and operational capabilities needed to move your programme forward faster.

An integrated approach to drug product development
Speak to our experts about your drug product development strategy today.