Core Capabilities
-
Development and production of controlled substances
-
Development of small molecule APIs and advanced intermediates
-
Patented manufacturing processes
-
Expertise in supporting development, submission and management of regulatory files (ASMF, CEP) for contracted customers
CordenPharma Cork R&D Center Capacities
Facility Legacy
CordenPharma Cork R&D Center’s core competencies consist of small-scale cGMP custom synthesis and development capabilities combined with extensive R&D services and full regulatory support.
Formerly a facility of Cambrex Corporation, CordenPharma Cork R&D Center brings over 15 years of experience in developing and producing controlled substances, small molecule APIs, advanced intermediates and patented manufacturing processes to the CordenPharma full-service CMO platform.
History
-
1974 – Set up as a new production site for APIs witih Boehringer Ingelheim Group
-
1992 – Sold to private equity group and established its presence in generic API and custom manufacturing business
-
1992-2009 Major experience and expertise in development, sale-up manufacture and registration of generic APIs
-
1999 – Sold to Cambrex Corporation (US)
-
2006 – Acquired by ICIG to become CordenPharma Cork Ltd
-
2009 – Closed manufacturing facility and relocated R&D operations to state-of-the-art laboratories nearby