研究合规

A key goal of 的 研究处 is to ensure that research, scholarship and creative activities 在上海州立大学进行的活动是安全、合乎道德和合法的. 研究办公室促进 的 meeting of this goal by coordinating 的 University’s 院校检讨委员会 (IRB) and 机构动物护理和使用委员会.

• Major equipment, infrastructure need, or radiation or laser use

  • Please 联系 following individuals guidance as early in 的 grant writing process :

    有关涉及激光的研究，请联系 大学激光安全主任.

    有关涉及辐射的研究，请联系 辐射安全主任.

    如果你r research will require 的 allocation of additional space or involve 的 purchase 需要专门安装的设备(如.g. 专用电路或水 lines)  联系 DROs (Director of 资源 and Operations) for your College.  

    
    如果你r research will require 的 renovation of your currently allocated space, contact 辛西娅·索托 在FD&O.  

• 研究利益冲突(COIR)

  • Your OSP Pre-Award Analyst should provide you with 的 necessary disclosures. 如果你 have questions about completing 的se disclosures, 联系 研究及合规小组.

• 人类遗骸

  • The procurement, use, transportation, and disposition of human remains or any o的r human materials in this category must be d一个 safely and respectfully. 此外, certain remains may be subject to additional federal and California State regulations. 如果你r RSCA activities involve human remains (whole body or body portion), human b一个s/b一个 fragments, or hair, teeth, or nails from deceased individuals you must 联系 研究服务高级总监 确认符合适用的法规.

• 美国缉毒署管制物质和列出的化学品

  • EH&S Department is responsible for ensuring that research or experiments involving controlled substances or listed chemicals complies with Drug Enforcement Agency regulations. Prior to possessing or working with DEA controlled substances, a Controlled Substance Use Authorization application must be 完成并提交给EH&S. 看到完整的 下列名单 U.S. Drug Enforcement 政府 (DEA) controlled substances 按时间表和 加州的易制毒化学品清单. 额外的 information and authorization applications can be obtained from 的 化学卫生主任 或者是 FD&O实验室安全网页.

• 机构动物护理和使用委员会

  • 协议表格张贴在 机构动物护理 & 使用委员会(IACUC). 此外, all investigators and personnel working on a project using animals must complete 的 necessary Animal Health and Welfare Training. IACUC验证 是否需要申请资助. 如涉及动物受试者，请联系 拉里年轻在你开始研究之前.

• 院校检讨委员会

  • A protocol must be submitted to 的 院校检讨委员会 (IRB). 我们建议 submission of 的 protocol package no later than sixty (60) days prior to 的 expected 合同日期. Information regarding 的 use of human subjects is posted at 的 IRB的网站, located at 人类受试者研究-机构审查委员会(IRB). 此外, all investigators using human subjects must complete 的 web-based tutorial which can be accessed at Web-based human subjects tutorial videos. 如果人类受试者是 涉及到的，一定要联系 IRB办公室 在你开始研究之前. 

• 院校生物安全委员会

  • 机构生物安全委员会(IBC) is responsible for ensuring that recombinant DNA research or experiments involving biohazardous materials are conducted in compliance with 国家卫生研究院, CDC Guidelines, and Cal OSHA Requirements to promote safe and responsible work practices. 在拥有之前， storing, or working with or transporting infectious agents, select agents, and toxins, human or nonhuman primate materials (including blood, body fluids, cells, and tissues), 重组DNA或转基因动物，联系 IBC的椅子 获得批准.

• 出口控制

  • 出口控制 Laws are a set of federal regulations that 政府ern how information and technologies can be transferred internationally and prohibit certain activities without 美国政府颁发的许可证. 采购研究设备，国际旅行， or sending data or technology to international collaborators can all trigger US export 控制. 联系 研究服务高级总监 to determine whe的r 菠菜网lol正规平台 must apply for a license on your behalf.

• 人类干细胞或胚胎组织

  • 如果项目涉及人类成体干细胞(e.g. 间充质干细胞，造血 stem cells, neural stem cells) or induced pluripotent stem cells (human somatic cells that are capable of dividing without differentiation in culture), 的 work requires review by a stem cell research oversight committee only if CIRM funds are being expended. If 的 project involves human embryonic stem cells, 的 research is covered by 的 California Health and 安全 Code, Section 125119(a)(1) and must be reviewed and approved by a stem cell research oversight committee 在你开始研究之前. 联系 的 研究服务高级总监 提交干细胞研究批准申请.

• 临床试验。

  • All clinical trials sponsored by 国家卫生研究院 must be registered on 临床试验.政府和 的 consent form posted to a public federal 政府ernment website. 此外，所有个体 responsible f或者是 design, conduct, or reporting of 的 clinical trial must complete 良好临床操作规范(GCP)培训. 你必须联络 研究及合规总监 在…上创建帐户 临床试验.政府. 

• 无人驾驶飞机

  • You will need to submit 的 make and model of 的 dr一个(s) being used, 的 plan for 使用，以及任何相关的许可信息 研究服务高级总监抄送, 上海外国语大学风险管理.

• 化学危害

  • EH&S is responsible for ensuring that research or experiments involving regulated or listed carcinogens, acute toxins, or extremely hazardous chemicals are stored, handled and disposed of safely as required by local, state or federal regulations. Prior to obtaining hazardous chemicals, a Chemical Procurement Request Form must be 完成并提交给EH&S. 你可以在这里找到表格 httpas possible://app.docusign.com/templates 通过搜索“EH”&S化学品采购申请表格. “单一”版本是 for 一个 product at a time, while 的 "multiple" version allows you to cover multiple 单个提交中的产品.在使用受管制的化学品之前， a Standard Operating Procedure (SOP) describing 的 storage, use, and disposal of regulated materials must be submitted to College 安全 Staff or EH&S. 额外的 信息可以从 化学卫生主任 或者是 FD&O实验室安全网页.

• 国际旅行

  • Traveling outside 的 United States on behalf of 的 University triggers additional 保险、IT安全和出口管制问题. 参观国际旅游 信息页或联系 研究服务高级总监 了解更多信息.