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ISO 13485 / ISO 14971 / ISO/TR 24971 - Medical Devices Package
ISO 13485 / ISO 14971 / ISO/TR 24971 - Medical Devices Package (Save 22% off List Prices)
Strengthen your medical device quality management and risk management processes with the ISO 13485 / ISO 14971 / ISO/TR 24971 Medical Devices Package. Designed for manufacturers, quality professionals, regulatory specialists, and compliance teams, this comprehensive collection combines the internationally recognized requirements of ISO 13485 with the practical implementation guidance of ISO 13485:2016 – Medical Devices – A Practical Guide. The package also includes ISO 14971 for medical device risk management and ISO/TR 24971, which provides detailed guidance on applying risk management principles throughout the product lifecycle. Whether you are developing new medical devices, maintaining regulatory compliance, preparing for certification, or improving your quality management system (QMS), this package delivers the essential standards and expert guidance needed to support product safety, regulatory compliance, and continuous improvement.
ISO 13485 / ISO 14971 / ISO/TR 24971 - Medical Devices Package includes:
International Organization for Standardization [iso]