Tailored to your specific drug product and market needs.
Leverage our expertise to help you transfer your existing products and processes from another contract development and manufacturing organization (CDMO). Our integrated approach makes it seamless to tech transfer from lab to pilot scale and up to commercial manufacturing.
Whether you need to manufacture a new commercial product or extend your commercial supply chain for an existing product, we have the experience to help you overcome the challenges of manufacturing highly potent APIs (HPAPIs).
We manufacture 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.
Expertise across all key areas of development, with analytical, manufacturing, quality, and regulatory support that helps mitigate risks and seamlessly tech transfer.