Cambrex announced an expansion of cGMP analytical testing capabilities at its site in Longmont, Colorado. Existing space at the site has been repurposed with cutting edge technologies and doubles the footprint of the laboratory operations. The world-class facility will gain approximately 1,800ft2 of laboratory space with a lean continuous improvement design deployed across the open module layout for efficiency. The expansion includes the addition of chromatographic equipment including uHPLC, HPLC, GC-FID/HS, and dissolution equipment (Apparatus 1 and 2 with online UV/Vis), as well as additional laboratory support equipment including 10 chemical fume hoods and working bench space. The Longmont facility became part of the Cambrex global network of development and manufacturing facilities following the acquisition of Avista Pharma Solutions in 2019. The site supports customers with the development and manufacture of small molecule drug substance and drug product and provides full analytical development and cGMP testing support from discovery through to clinical scale. The site is fully integrated with direct technical transfer lines for commercial scale advancement to the Charles City, Mirabel, and Whippany sites.