World Class Manufacturing
Beginning with process and analytical development and optimization, continuing with clinical-scale volume, and scaling up customers’ APIs following regulatory approval, Purisys assists customers at every phase of commercial development. Our manufacturing is supported by our extensive reference standards portfolio and analytical capabilities.
We manufacture these ingredients at high-capacity cGMP commercial production facilities in Europe and the United States. If you are developing pharmaceuticals toward regulatory approval in more than one country or region, you can partner with Purisys for global supply solutions. cGMP production is in place in Europe and the United States, making export and import of your APIs to the country of your choice fast, secure and in regulatory compliance.
A Secure Pharmaceutical Supply Chain
Pharmaceutical manufacturers that partner with Purisys get superior supply chain security. High-quality raw materials for the manufacture of API’s is specifically dedicated at the start of any partnership, along with dedicated API production capacity, and secure delivery of APIs in full compliance with DEA import and export rules. GMP manufacturing in the US and EMEA provides Purisys with true global reach to customers within a multitude of market sectors.