DQS India is organizing ISO 14971 Risk Management Training for Medical Devices
ISO 14971:2019 defines the international requirements of risk management systems for medical devices, defining best practices throughout the entire lifecycle of a device. To ensure your organization brings a compliant product to market efficiently and safely, you need to successfully implement a risk management system.
- Key Requirements of ISO 14971:2019 standard
- Regulatory Requirements
- Risk Management and the Medical Device Regulations (MDR)
- Understanding the linkages between ISO 14971:2019, ISO 13485:2016 & MDR 2017/745
- Application of Risk Management to Medical Devices
- Course Review & feedback
Auditors
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Girish Silswal
Moderator
Director & Head-Management System Assurance Business at DQS India