In this episode of the MedTech Innovation 360, we delve into risk assessment and management within medical device development. Exploring the definitions of risk, we differentiate between risk assessment and risk management, stressing the importance of early identification and mitigation. Key points include the relationship between risk and hazards, the role of Failure Modes Effects Analysis (FMEA) in identifying potential failures, the significance of ISO 14971 as a guiding standard, and the integration of user and design perspectives in comprehensive risk analysis. Practical examples, such as sidewalk cracks, illustrate risk analysis criteria. We also emphasize considering manufacturing processes and material properties for product safety and functionality. Throughout, we employ real-world analogies and detailed examples to make complex concepts accessible, aiming to help medical device professionals enhance product safety and efficacy through meticulous risk analysis and proactive design adjustments.
#8 Strategic Risk Management in MedTech Innovation
44:13
#7 FDA Regulations Guide for Medical Device Developers
41:10
#6 The Power of Marketing in the Medical Device Industry
45:24
#5 Compliance Matters: Navigating FDA Clearance and ISO Certification for Medical Devices
50:00
#4 The Art of Innovation: How Industrial Design Shapes Medical Devices
48:09
#3 Unleashing the Power of Industrial Design
46:51
#2 Best Practices for Conducting User Research in Medical Device Development
45:47
#1 Designing for Patients: The Power of User-Centered Medical Device Development
31:28