Accelerate the path from proof-of-concept to commercial launch.
We have over 30 years of global experience, and are a trusted partner in providing the expertise to get life-saving medicines to patients, faster.
Our unique integrated approach makes it seamless to transfer technology from lab scale to pilot scale to commercial manufacturing. We can easily transfer existing products and processes from another contract development and manufacturing organization (CDMO).
Whether you need to manufacture a new commercial product or extend your commercial supply chain for an existing product, we have the experience and capabilities to help you overcome the challenges that highly potent APIs (HPAPIs) pose and minimize risk.
Our global, state-of-the-art global facilities are ready for your pharmaceutical commercial manufacturing challenge.
We can support all aspects of your drug product supply for Phase III clinical studies and commercial supply. That includes the manufacture of all oral drug product dosage forms in our US Food and Drug Administration (FDA)-, European Medicines Agency (EMA)-, and Japanese Pharmaceuticals and Medical Devices Agency (PMDA)-approved facilities.
We have expertise across all key areas; development, analytical, manufacturing, quality, and regulatory. We will help to mitigate risks and can seamlessly transfer existing products and processes, minimizing risk.