Instrument Benefits

Precision micro-filling of API into capsules – equates to low waste of API

Records the weight of drug in each capsule – allowing traceability of samples that meet GMP requirements

Removes the need for excipients that are normally required for filling purposes and associated stability studies

Faster time to ‘first-in-human’ studies

Products to suit both pre-clinical, clinical trial filling requirements and small-scale product manufacturing

Eliminates drug/excipient compatibility issues

Reduces pre-formulation time and effort

Creates flexibility needed for dose ranging doses

Simplifies development of drug product stability indicating assays

Simplifies stability protocols

Drug substance is fully retrievable

Minimizes drug loss