Sterile and Non-sterile production

Steril ve Non-steril Üretim

As an Analysis Clean Room, rooms with ISO, USP, GMP and FDA compliant cleanliness and pressure levels are created. During sterile preparation, laboratories and manufacturers need materials and devices for the storage, manufacture, packaging of drugs, as well as for the removal of waste and used materials. The analysis ensures that life sciences facilities remain compliant with standards and regulations by following strict protocols for cleanliness and sterility in Cleanroom installations, and aseptic isolators (CACs), modular cleanrooms, Class II B2 biosafety cabinets, material transfer cells and ISO 5 compliant cleanrooms for pharmaceutical manufacturing facilities supplies materials and devices such as equipment.