徕博科（Labcorp）宣布，其首款获得美国食品药品监督管理局（FDA）批准的基于RNA技术的居家结直肠癌筛查检测产品Colosense®，现已在美国全国范围内上市。这款创新的非侵入性检测工具，标志着结直肠癌早期筛查领域的一次重要突破，为公众提供了更为便捷、私密的筛查选择。
徕博科（Labcorp）宣布，其首款获得美国食品药品监督管理局（FDA）批准的基于RNA技术的居家结直肠癌筛查检测产品Colosense®，现已在美国全国范围内上市。这款创新的非侵入性检测工具，标志着结直肠癌早期筛查领域的一次重要突破，为公众提供了更为便捷、私密的筛查选择。
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