首页> 外文期刊>Cytotherapy >Development of advanced therapies in Italy: Management models and sustainability in six Italian cell factories
【24h】

Development of advanced therapies in Italy: Management models and sustainability in six Italian cell factories

机译:在意大利开发先进疗法:六个意大利细胞工厂的管理模式和可持续性

获取原文
获取原文并翻译 | 示例
           

摘要

On November 10, 2014, the representatives of all six certified Good Manufacturing Practices (GMP) cell factories operating in the Lombardy Region of Italy convened a 1-day workshop in Milan titled "Management Models for the Development And Sustainability of Cell Factories: Public-Private Partnership?" The speakers and panelists addressed not only the many scientific, technological and cultural challenges faced by Lombardy Cell Factories, but also the potential impact of advanced therapy medicinal products (ATMPs) on public health and the role played by translational research in this process. Future perspectives for research and development (R&D) and manufacturing processes in the field of regenerative medicine were discussed as well. This report summarizes the most important issues raised by the workshop participants with particular emphasis on strengths and limitations of the R&D and manufacturing processes for innovative therapeutics in Lombardy and what can be improved in this context while maintaining GMP standards. The participants highlighted several strategies to translate patient-specific advanced therapeutics into scaled manufacturing products for clinical application. These included (i) the development of a synergistic interaction between public and private institutions, (ii) better integration with Italian regulatory agencies and (iii) the creation of a network among Lombardy cell factories and other Italian and European institutions.
机译:2014年11月10日,在意大利伦巴第大区运营的所有六家获得认证的良好生产规范(GMP)电池工厂的代表在米兰召开了为期1天的研讨会,主题为“细胞工厂发展和可持续性的管理模型:私人伙伴关系?”演讲者和小组成员不仅讨论了伦巴第细胞工厂面临的许多科学,技术和文化挑战,而且还讨论了先进治疗药物产品(ATMP)对公共卫生的潜在影响以及转化研究在此过程中所发挥的作用。还讨论了再生医学领域的研究与开发(R&D)和制造过程的未来前景。本报告总结了研讨会参与者提出的最重要的问题,尤其着重于伦巴第创新疗法的研发和制造工艺的优势和局限性,以及在保持GMP标准的同时可以改进的方面。与会者重点介绍了几种将患者特定的先进疗法转化为规模化制造产品以用于临床的策略。其中包括(i)发展公共和私人机构之间的协同互动,(ii)与意大利监管机构更好地整合,以及(iii)在伦巴第细胞工厂与其他意大利和欧洲机构之间建立网络。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号