areta provides filling and final finishing of bulk products manufactured in house or provided by the customer. areta’s methodology offers filling capabilities with very low dead volumes starting from small clinical batches. The process is carried out in EU grade A with a grade B environment of areta’s GMP facility.

The environment monitoring of laminar flow hoods, rooms and operators, is monitored as described in the Annex 1 (Manufacture of Sterile Medicinal Products). areta provides filling and final finishing of bulk products manufactured in house or provided by customer.