[Free] Iso 14971 Applied Medical Device Risk Management Course
Become a Risk Management Expert in ISO 14971:2019 – Free Course
What you’ll learn
- Master the Foundations of Medical Device Risk Management
- Develop and Implement Risk Management Processes in Compliance with Regulatory Standards
- Identify, Assess, and Control Risks with Advanced Analytical Techniques
- Utilize Design Controls and Systems Engineering to Enhance Device Safety
Requirements
- No Prior Experience Required This course is designed for both beginners and professionals, so no prior experience in medical device development or risk management is necessary. A strong interest in learning about medical devices, regulatory requirements, safety management and systems engineering will enhance your experience, as the course dives into this indepth.
Description
Are you ready to master ISO 14971 and transform your understanding of medical device risk management? Designed specifically for working professionals, ISO 14971 Applied Medical Device Risk Management will empower you to confidently apply risk management principles in the design and development of medical devices, giving you the knowledge and skills to ensure compliance and patient safety. Navigating the complexities of ISO standards can be daunting, but this course breaks down ISO 14971 into clear, actionable insights, making it accessible—even if you’re new to risk management. By the end, you’ll not only understand the core principles of risk management but also gain practical skills to apply them in real-world scenarios. This isn’t just a course on theory; it’s a hands-on, practical approach to turning ISO 14971 requirements into effective practices that enhance your device’s safety and compliance.What can you expect from this course? We’ll start by covering foundational concepts such as key definitions, the relationship between ISO 14971 and ISO 13485, and the risk-benefit analysis of medical devices. You’ll learn the essentials of hazard identification, risk assessment, and risk control. Dive into advanced topics like design controls, traceability, and how to integrate risk management into systems engineering and architecture for robust device design.
Throughout the course, we emphasize a systematic approach to identifying hazards, estimating and evaluating risks, implementing risk control measures, and verifying their effectiveness. We’ll also discuss managing residual risk and ongoing risk management during production and post-production, ensuring you’re equipped to handle every stage of the risk management lifecycle.
By the end of this course, you’ll be able to:
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Simplify and implement ISO 14971 requirements with confidence
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Conduct thorough risk assessments and apply effective risk control measures
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Integrate risk management seamlessly into the product development process
This course offers you a powerful transformation: from potentially feeling overwhelmed by regulatory standards to becoming a confident, informed professional who can apply risk management practices that not only protect patients but also elevate your organization’s product quality and compliance. Join now and take the first step toward mastering ISO 14971.
Patient safety and regulatory compliance start with effective risk management.
Author(s): Robert Ryan
