Almac has expands its pharmaceutical development services with the creation of a new facility at our UK headquarters in Craigavon.

With an initial investment of £4.5million, phase one of the expansion will provide a state-of-the-art, non-GMP formulation development facility for the development and scale-up of solid oral dose drug products using a broad range of technologies. 

The new formulation development suites will complement Almac’s existing pharmaceutical development facilities and will include high levels of control over environmental conditions as well as extending current capabilities in processing high-potent compounds.

The current GMP development facilities focus on drug products up to pilot scale & registration, whereas, the new facility will operate at lab-scale, with batch sizes for most technologies typically expected to be less than 15 kg scale. 

Phase two of the project will involve a significant expansion of GMP analytical support capabilities with the construction of 2 additional QC laboratories within the new facility.

 “The new facilities will effectively double our current pharmaceutical development capacity allowing us to meet the growing demand for our services, both from existing and new clients.  Recruitment of experienced formulation and analytical development staff has already commenced in support of this exciting expansion” stated John McQuaid, VP of technical operations.

Phase one of the expansion is due for completion mid 2012 with phase two of the expansion and configuration of dedicated analytical labs completing towards the end of 2012.