Скачать или смотреть How Does ISO 14971 Apply To Medical Device Risk Management? - How It Comes Together

How Does ISO 14971 Apply To Medical Device Risk Management? Are you curious about how medical devices are kept safe for patients and users? In this video, we’ll explain the key role of ISO 14971 in managing risks throughout the entire life cycle of medical devices. We’ll cover the essential steps involved in risk management, from initial planning and hazard identification to implementing safety controls and verifying their effectiveness. You’ll learn how manufacturers assess and reduce potential hazards like electrical issues, software glitches, or material concerns to ensure devices perform safely during normal use. We’ll also discuss the importance of ongoing monitoring and how this standard works alongside quality management systems such as ISO 13485 to promote consistent safety practices. Whether you’re involved in medical device development, quality assurance, or regulatory compliance, understanding ISO 14971 is vital for creating safer products and meeting global standards. Join us as we break down the process of risk management in medical device manufacturing and discover how manufacturers strive to deliver safe, reliable devices for patients worldwide. Don’t forget to subscribe for more insights into medical device safety, standards, and regulations!

⬇️ Subscribe to our channel for more valuable insights.

🔗Subscribe: https://www.youtube.com/@HowItComesTo...

#MedicalDeviceSafety #RiskManagement #ISO14971 #MedicalDevices #PatientSafety #RegulatoryCompliance #QualityManagement #MedicalManufacturing #DeviceSafety #RiskAssessment #HealthcareInnovation #MedicalStandards #SafetyControls #PostMarketMonitoring #MedicalRegulations

About Us: This is where our about us goes