The Germany-based cleanroom specialist has actually finished the job for leading blister product packaging service provider Blisterzentrum
Image credit: CAT Clean Air Technology
CAT (Clean Air Technology) Group has actually completed a cleanroom growth for among the biggest professional business for device blister product packaging; Blisterzentrum Baden-Württemberg in Magstadt.
Mechanical blister product packaging is among the most modern-day types of drug supply. Approved completed medical items are repackaged under cleanroom conditions in accordance with EU GMP standards – on a patient-specific basis in accordance with medical medication strategies. Blisterzentrum has considerably broadened its cleanroom capabilities. On an overall of 100 sqm of Class D cleanroom space, the business now loads 10s of countless blister bags every day and materials numerous thousand clients. The production of the secondary blisters in the cleanroom ensures the greatest requirement of health.
The scope of the agreement likewise consisted of a couple of ‘specials’ that required a great deal of coordination from the trades included throughout continuous operations – consisting of the development in between the existing and growth locations, the setup of a dust barrier and the setup of a brand-new ventilation system
“We had the ability to carry out the whole growth job for our consumer: from preparing to job coordination and cleanroom equipment to preliminary and requalification procedures,” CAT Group mentioned. “The scope of the agreement likewise consisted of a couple of ‘specials’ that required a great deal of coordination from the trades included throughout continuous operations – consisting of the development in between the existing and growth locations, the setup of a dust barrier and the setup of a brand-new ventilation system.”
CAT Clean Air Technology GmbH, headquartered in Stuttgart, is a prominent global cleanroom service provider. Since it was established in 1995, the business has actually made sure that cleanrooms, with all their systems are appropriately prepared, developed, accredited after conclusion and frequently kept an eye on in day-to-day operation. Exactly as recommended by the GMP, FDA, VDI or ISO standards.
