Recently the API's Finishing Department has been rebuilt to meet current pharmaceuticals finished dosage form standards and room classification/material flow requirements.
All equipment (Centrifuges,Filters,Rotative and Static Dryers,Mills,Sieves,etc) are installed in Clean Rooms,in order to avoid any possible internal,external and cross contamination.
Clean rooms, where the process material is exposed, e.g for charging operations are designed to have an ISO7 classification (grade C,with class 1000:the maximum permitted number of 0.5μm particles is 35000 p/m³).Such rooms are at highter pressure than adjoining rooms of lower classification,to prevent product migration through openings.
Solid Isolation
Solid Drying
7 Centrifuges
Stainless Steel and Acid-Resistant
(installed in clean room Class C)
7 Static - Air and Under Vacuum Dryers
(discharging product in clean room Class C)
2 Fully automated Filter Dryers
(installed in clean room Class C)
1 Stainless Steel Double Cone Rotary Dryer
(discharging product in clean room Class C)
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1 Glass-Lined Double Cone Rotary Dryer
(discharging product in clean room Class C)
Product finishing
Versatile milling and sieving equipments-Pharmaceuticals grade
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LUPI Lundbeck Pharmaceuticals Italy S.p.A. Via Quarta Strada 2 35129 Padova - Italy
