In the United States, the maintenance and calibration of biomedical equipment are guided by standards and best practices set forth by organizations such as the FDA, The Joint Commission, Centers for Medicare & Medicaid Services (CMS), and the AAMI. These regulations require that all electrical and mechanical biomedical equipment undergo regular preventive maintenance and calibration according to the manufacturer’s recommendations and applicable quality control procedures.
All procedures are fully standardized and comply with current regulatory requirements to ensure safety, performance, and compliance.
Additionally, our advanced software allows us to track and analyze equipment performance across multiple years, ensuring accurate records and timely interventions for continuous improvement.