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《人胚胎干细胞》标准落地,细胞有望成为“活药品”
发布时间:2019-03-18   点击次数:123次

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“干细胞产业必将过渡到能够标准化生产、规模化制备阶段,实现可监管、可重
复、可验证的临床应用产品生产,不能停留在无法证明安全性、有效性的临床研究阶段。”周琪表示,胚胎干细胞在未来可能会成为干细胞药物研发领域重要的原料,这意味着需要“标准先行”。随着标准制定工作的细化、基础研究的深入、临床研究的推进,细胞制品进入临床也将会拥有均一性、稳定性等特质。

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