In the Injectable Cephalosporin Department, structured as a separate entity, completely independent from non beta-lactam manufacturing areas, micro powder filling under aseptic conditions is performed in accordance with all current Good Manufacturing Practice (cGMP) requirements. Manufacturing conditions are being continuously monitored through computer-supported systems.
The facility is further supported by cold storage rooms completely dedicated to these products.
The cartoning of the vials destined to local and international markets also takes place in the Injectable Cephalosporin Department.
