INBIT helps hospitals safeguard patients, support clinical teams, and manage medical device risk with confidence. Through structured safety testing, continuous vigilance, and expert regulatory support, we enable healthcare organizations to meet their obligations while ensuring that medical devices perform safely and reliably throughout their lifecycle.
Our services focus on the areas where safety matters most: critical care environments, patient-connected equipment, and high-risk medical technologies. By combining proactive testing with real-time monitoring of safety alerts, adverse incidents, and recalls, we help hospitals identify risks early and take timely, informed action.
With more than 20 years of active involvement in European and international medical device safety initiatives, INBIT brings trusted expertise and access to global vigilance intelligence. This allows us to provide clear, actionable guidance that reduces operational and legal exposure while strengthening patient and staff protection.
Partnering with INBIT means greater assurance in the safety of medical technology and greater confidence in healthcare delivery.
Patient & Staff Safety
Ensuring the safe operation of medical devices to protect patients, clinicians, and healthcare teams.
Risk Identification & Mitigation
Early identification of devices associated with reported incidents and clear guidance on corrective actions.
Electrical & Functional Safety Testing
Regular testing of medical equipment, with emphasis on critical care areas and patient-connected devices.
Regulatory Compliance Support
Alignment with EU medical device regulations, supporting hospitals in meeting their legal and safety obligations.
Medical Device Vigilance & Recalls
Continuous monitoring of safety alerts, adverse incidents, and recalls at European and international level.
Trusted Expertise
Over 35 years of active involvement in European and international medical device safety initiatives.