API process development & scale-up

• Route scouting • Feasibility studies • Synthesis of compounds in mg/g scale • Metabolite synthesis • Preparation of standards / reference substances • Impurity profiling • Impurity reference synthesis • Synthesis of stable isotope labelled substances

• cGMP manufacturing of APIs and key intermediates • Analytical method validation • Process validation • ICH stability studies • Degradation studies • Full CMC package • Drug master files: compilation, maintenance • Comprehensive documentation

Pharmatory people

Our employees form a compact and efficient group of highly motivated pharma professionals working as though parts of the customer organisation towards our shared goal. The spirit of supporting others and sharing the values is readily reflected in the results of our work.

Competitive advantage is sustained by having the appropriate skills to deliver business objectives. Our goal is to establish an environment that facilitates learning and ensures the levels of training and competence by local regulation. Our staff training program is specified by SOP and reviewed for every employee in annual performance discussions.