You're caught in a tough place. As a biomedical engineering, clinical governance, quality management, or risk management professional, you're responsible for patient safety at a time when demands for greater efficiency and even cost reductions are growing.
To make things worse, innovation is a two-edged sword. Medical devices designed to manage chronic, non-communicable diseases are increasingly instrumented, interoperable, connected and intelligent. While such innovations allow patients to better manage their health on a day-to-day basis with oversight from their clinicians, there's also a higher likelihood of adverse events when things go wrong, harming patients and putting your organisation on the line to recognize and respond quickly.
When something bad happens, it's challenging. You find yourself sifting through a sometimes maddening mix of data, documents, workflows and systems - inside your walls and working with suppliers and partners. With the clock ticking, you scramble to track and trace all of your devices and execute a rapid, targeted and thorough remediation and/or removal plan.
Where to Turn?
At Spiritus, we understand and we're here to help. Learn more by contacting us today.