Close
Patheon

Brochures

Corporate

  • Patheon is transforming the way pharmaceuticals are made with a simplified, end-to-end supply chain for pharmaceutical and biopharmaceutical companies of all sizes. Drug substances and drug products. Development and manufacturing. Small and large molecules. Sterile, oral solid and softgel dosage forms. Patheon offers a comprehensive range of services spanning all phases and scales that is wider and deeper than any other CDMO....View More

    more...
  • Take months off the development timelines of your large and small molecule discoveries. With Patheon OneSource™ you can combine your drug substance and drug product development and manufacturing into a single customized solution to simplify your supply chain and accelerate your discovery to proof of concept....View More

    more...

Biologics

Small Molecule API

  • Take a big picture approach to small molecules. Ensure that you always have the exact resources and expertise you need, especially for your most difficult to manufacture compounds. With Patheon you’ll have access to a vast array of small molecule API capabilities in Europe and the United States....View More

    more...
  • Phase I clinical materials in as little as 12 weeks. Only twelve weeks from receipt of your API, Patheon Quick to Clinic™ can deliver bulk clinical trial materials for first-in-human studies. That includes a one-month stability study so you have all the data you need to make informed proof of concept decisions and complete regulatory submissions. What’s more, this accelerated program gives you the choice of five dosage forms....View More

    more...

Commercial Product Supply

  • Access a remarkable range of conventional and specialized oral solid dosage form capabilities and scale. Tap the many clinical and technical advantages of softgels with a host of patent-protected specialized technologies. Access Extensive sterile pharmaceutical development and manufacturing capabilities at all scales....View More

    more...

Product Development

  • Not addressing solubility at the beginning of development can put your timeline and your molecule at risk. As many as 60-90% of drug candidates have bioavailability challenges and 37% will fail in phase I-III clinical trials as a result....View More

    more...
  • What’s the best path for your low soluble molecule? Two molecules, both designed to treat the same condition, both with solubility challenges. Two biopharma companies racing to be first. Biopharma A chooses to move into trials as quickly as possible, while Biopharma B decides to address broader solubility concerns first. Who gets to market first may surprise you....View More

    more...
  • Under pressure to minimize costs and timelines during clinical development, it’s become common to put off solubility challenges. However, with 60%–90% of today’s new molecular entities presenting as insoluble, it makes sense to reconsider this strategy and its significant risks....View More

    more...

Media Contact

Mari Mansfield
4815 Emperor Blvd.,
Durham, NC 27703
(919) 226-3137
mari.mansfield@patheon.com

 
 

Media Contact

Mari Mansfield
4815 Emperor Blvd.,
Durham, NC 27703
(919) 226-3137
mari.mansfield@patheon.com