Stipulations on de-identification and scientific research in the European General Data Protection Regulation (GDPR) help research organizations to use personal data with fewer restrictions compared to data collection for other purposes. Under these exemptions, organizations may process specific...

1. Introduction to medical device requirements -- 2. Preventing recalls during specification writing -- 3. Risk assessment and risk management -- 4. Preventing recalls during early design -- 5. Preventing recalls during the detail design phase -- 6. Designing for prognostics to protect patients...

The growth of remanufacturing has seen its application in different industrial sectors including automotive, electronics and medical devices. In medical and healthcare sector, remanufacturing presents an opportunity to equip facilities with functional, safe, affordable and sustainable medical...

Medical device firms operate at the frontiers of innovation. When functioning properly, innovative medical devices can prolong and improve lives; when malfunctioning, the same devices may harm patients and lead to product recalls. Product recalls create significant challenges for firms, but...

The purpose of this study is to identify the factors impacting medical professionals' adoption intention of AI-based innovative medical devices focused on the mediating role of trust. Drawing on the UTAUT model, we examined the mediating effect of trust in the relationships between these factors...