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Published March 30, 2015
Will install a new Class 100,000 suite at its North East England facility Read More »
Published March 23, 2015
Adds 2,050 sq. ft. of cleanroom suites with dedicated air handling for potent compounds Read More »
Published March 9, 2015
Streamlines manufacturing ops into Athlone and Wilmington facilities Read More »
Published September 3, 2014
Will test commercial drug product for the European market Read More »
Published June 26, 2014
Enables CTM services in more than 44 Asian countries Read More »
Published June 12, 2014
Will manufacture Phase IIb batches of Ovasave for Crohn’s trial Read More »
Published June 5, 2014
Will reinstate GMP certificate Read More »
Published October 5, 2012
What level of GMP need to be followed for clinical trial materials (for a generic ANDA) intended for animal studies if the drug is already in the market? Read More »
Published February 27, 2012
See Good Manufacturing Practice.… Read More »
Published April 1, 2015
Granted authorization to produce lentiviral vectors for clinical use and CAR-T cell therapies Read More »


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