"Medical Devices Regulatory Aspects: A Comprehensive Guide" provides a clear and concise overview of the regulatory frameworks governing medical devices and in vitro diagnostics worldwide. This essential resource covers key regulatory processes, international standards, and compliance strategies for major markets, including the United States, European Union, and Asia. Designed for studets, regulatory professionals, manufacturers, and researchers, this guide offers practical insights and real-world examples to navigate the complexities of medical device regulation. Enhance your understanding and ensure compliance in the ever-evolving field of medical technology with this comprehensive and accessible guide.
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Hardcover. Zustand: new. Hardcover. "Medical Devices Regulatory Aspects: A Comprehensive Guide" provides a clear and concise overview of the regulatory frameworks governing medical devices and in vitro diagnostics worldwide. This essential resource covers key regulatory processes, international standards, and compliance strategies for major markets, including the United States, European Union, and Asia. Designed for studets, regulatory professionals, manufacturers, and researchers, this guide offers practical insights and real-world examples to navigate the complexities of medical device regulation. Enhance your understanding and ensure compliance in the ever-evolving field of medical technology with this comprehensive and accessible guide. This item is printed on demand. Shipping may be from multiple locations in the US or from the UK, depending on stock availability. Bestandsnummer des Verkäufers 9798894154695
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Hardcover. Zustand: new. Hardcover. "Medical Devices Regulatory Aspects: A Comprehensive Guide" provides a clear and concise overview of the regulatory frameworks governing medical devices and in vitro diagnostics worldwide. This essential resource covers key regulatory processes, international standards, and compliance strategies for major markets, including the United States, European Union, and Asia. Designed for studets, regulatory professionals, manufacturers, and researchers, this guide offers practical insights and real-world examples to navigate the complexities of medical device regulation. Enhance your understanding and ensure compliance in the ever-evolving field of medical technology with this comprehensive and accessible guide. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability. Bestandsnummer des Verkäufers 9798894154695
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Hardcover. Zustand: new. Hardcover. "Medical Devices Regulatory Aspects: A Comprehensive Guide" provides a clear and concise overview of the regulatory frameworks governing medical devices and in vitro diagnostics worldwide. This essential resource covers key regulatory processes, international standards, and compliance strategies for major markets, including the United States, European Union, and Asia. Designed for studets, regulatory professionals, manufacturers, and researchers, this guide offers practical insights and real-world examples to navigate the complexities of medical device regulation. Enhance your understanding and ensure compliance in the ever-evolving field of medical technology with this comprehensive and accessible guide. This item is printed on demand. Shipping may be from our Sydney, NSW warehouse or from our UK or US warehouse, depending on stock availability. Bestandsnummer des Verkäufers 9798894154695
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