Hillerod, Denmark

The Hillerød, Denmark site is a 50,000 square foot facility designed for solid and liquid-phase development and large scale GMP manufacture of large scale intermediates.

The Hillerød facility consists of 1 multi-purpose synthesis area (solid and solution phase), 3 purification suites, and one classified isolation suite with lyophilization capacity up 200 kg (ice capacity). With solid-phase reactors of up to 280 L in size, and HPLC columns with internal diameters of up to 60 cm, Hillerød is equipped to produce batches in quantities of up to ten-kilogram lots.

The Hillerød site  has successfully undergone 6 inspections by the Danish national regulatory authorities and had a successful pre-approval inspection by the US FDA in 2013. 

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