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This comprehensive handbook serves as an essential guide to the scientific, technical, and clinical evaluation of biomaterials, with a specific focus on the rigorous testing of implant materials. It provides professionals with critical insights into methodologies, international standards, and regulatory requirements necessary for assessing the safety and performance of medical implants, reflecting the most current knowledge in its second edition.

Effective regulation of medical products is essential for safeguarding public health, ensuring the efficacy and safety of pharmaceuticals, medical devices, and diagnostic tools. This comprehensive oversight involves navigating complex national and international guidelines governing research, development, manufacturing, distribution, and post-market surveillance, all crucial for responsible innovation and consumer trust.