GRIFOLS
KIRO Fill, designed for sterile medication preparation of non-harmful drugs; It includes touch screen for user instructions and approvals, barcode and RFID systems to identify and control the source and end containers used.
Features
Security
Control and Traceability
Flexibility and Efficiency
Regulatory Compliance
Compliance with supported USP and GMP regulations by standardizing aseptic procedures, facilitating personnel and process qualification,
Airflow operation and temperature control and optional continuous particle counter to meet GMP requirements,
Fully maintained during deployment, qualification, and periodic maintenance, including dosing accuracy tests and airflow certifications addressing smoke tests under dynamic conditions for USP compliance,
KIRO Oncology meets electrical safety requirements with UL listing marked according to IEC 61010 and EMC certification according to IEC 61326-1.
Automatic Drug Preparation Device
Automatic drug preparation devices are used for sterile preparation of sterile and unclean ready-made drugs. Traceability is achieved by using a barcode/data matrix and RFID systems that identify and control the last source and containers used.
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