Core 4: Regulatory Compliance

核心4：合规性 摘要 监管合规核心(RCC)服务于促进医疗行业的高级发展 针对需要最大限度遏制的病原体的对策。这包括旨在评估 通过评估对拟通过美国食品和药物管理局提交的动物模型进行疗效评估 (FDA)动物规则，或旨在根据FDA良好实验室规范(GLP)评估安全性的研究 规章制度。连同在赞助商同意的质量体系下进行的研究，这些是 被认为是“有据可查的研究”。RCC由一个非临床研究单位组成，即 负责进行研究，并由一个独立的质量保证股监督 确保遵守法规的研究。农村信用社的具体目标是：1.发展和完善 开展有良好记录的研究、回应审核并持续改进 程序；2.监控记录良好的研究，以确保在此过程中生成的任何数据的准确性和完整性 研究；3.对相关人员进行有文件记录的相关合规培训；4.制定政策 以及与监管合规核心有关的程序。RCC是所有利益相关者的支点 参与完成有案可查的研究。研究的关键参与者包括：校长 调查员、研究主任(SD)、研究控制点(SPOC)；质量保证；测试设施 管理(TFM)；波士顿大学领导层；赞助商；实验室；兽医工作人员；设施 维护；和生物安全。协调一项有充分记录的研究依赖于紧密的整合和 从早期和频繁的沟通开始。研究的PI，GLP的SD，或动物规则的SPOC， 质量保证股的成员在提案制定阶段开始讨论项目。 这确保了可行性得到考虑，包括对主计划的考虑，并且风险是 减刑。特别是，发起人最好同意一项研究的质量计划 GLP-要求；SD/SPOC、PI和质量保证部门密切合作以制定这些计划。作为 议定书将进一步制定，其他利益攸关方也将参与讨论。所有各方都参与其中 在研究的执行过程中，RCC确保在研究完成后进行总结经验教训的讨论。

Core 4: Regulatory Compliance Abstract The Regulatory Compliance Core (RCC) serves to facilitate the advanced development of medical countermeasures for pathogens that require maximum containment. This includes studies aimed to evaluate efficacy by evaluation in animal models intended for submission via the US Food and Drug Administration (FDA) Animal Rule, or studies aimed to evaluate safety following the FDA Good Laboratory Practice (GLP) regulations. Together with studies that are performed under a Quality System agreed with a sponsor, these are considered “Well Documented Studies.” The RCC is comprised of a Nonclinical Studies unit, that is responsible for the conduct of studies, and an independent Quality Assurance Unit provides oversight of those studies to assure compliance with regulations. The specific aims of the RCC are to: 1. Develop and refine the processes required to carry out Well-Documented studies, respond to audits, and continually improve the program; 2. Monitor Well Documented studies for accuracy and integrity of any data generated in such studies; 3. Conduct relevant Well Documented compliance training for relevant personnel; 4. Develop policies and procedures pertaining to the Regulatory Compliance Core. The RCC is the fulcrum for all the stakeholders involved in the accomplishment of Well Documented Studies. Critical participants in studies include: Principal Investigators, Study Directors (SD), Study Point of Control (SPOC); Quality Assurance; Test Facility Management (TFM); Boston University Leadership; Sponsors; Laboratorians; Veterinary staff; Facility maintenance; and Biological safety. Coordination of a Well Documented study relies on tight integration and begins with early and frequent communication. The PI of a study, the SD for GLP, or SPOC for Animal Rule, and members of the Quality Assurance Unit start discussing a project during the proposal development stage. This assures that feasibility, including consideration of the Master Schedule, are considered and risks are mitigated. In particular, it is preferred that a sponsor agrees to a Quality Plan for a study that does not have a GLP-requirement; the SD/SPOC, PI, and Quality Assurance Unit work closely to develop these plans. As the protocol is developed further other stakeholders are incorporated into the discussions. All parties are involved in the execution of a study, and RCC assures a lessons-learned discussion occurs following study completion.