Our Offer for Large Pharmaceutical Companies
Eurofins CDMO (Contract Development and Manufacturing) provides the full range of integrated API and Drug Product outsourcing services. Over the last thirty years, we have worked for large pharmaceuticals companies on global projects through our facilities in North America, Europe and Asia.
Services at a glance:
- Small molecule development and manufacturing
- Biologics development and manufacturing
- Formulation Development of oral, parenteral, topical and nasal form including lyophilization
- Development of Drug Product (tablets and capsules in blisters and bottles, topical forms in bottles or tubes, parenteral in vials and PFS)
- Non-sterile manufacturing including double blind management and manufacture of placebo
- Aseptic manufacturing (fill/finish)
- Clinical trial materials, packaging & logistics including Direct to Patient Service
With state-of-the-art facilities in Canada, Europe and India and global regulatory expertise, Eurofins CDMO provides high-quality, customized solutions for complex products and unique production processes, specializing in the development of innovative formulation technologies and solutions to enhance bioavailability and control drug release for difficult-to-formulate drug candidates.
Why should you select us:
✔ Consolidate vendors to move rapidly through the drug development value chain
✔ Navigate complex formulation screening and development
✔ Accelerate process development and scale-up for API & Drug Product
✔ Oversee drug life-cycle management
✔ Ensure regulatory compliance throughout each stage of the development cycle
