Reference standards play a crucial role in the field of Anti-Cancer/Oncology by providing a benchmark for accurate and reliable measurement of various parameters. These standards serve as a reference point for the development, validation, and quality control of diagnostic tests, drugs, and therapies used in the diagnosis and treatment of cancer. They help ensure consistency and comparability of results across different laboratories and research studies, enabling effective communication and collaboration among healthcare professionals and researchers. By establishing standardized methods and materials, reference standards enable accurate and precise measurement of cancer biomarkers, genetic mutations, drug efficacy, and toxicity, thereby facilitating the development of new therapies, monitoring treatment response, and improving patient outcomes in the fight against cancer.

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