人类受试者研究

1. 与你的资助机构(NIH, NSF等)核实.)的内部审核时间要求 批准.
2. Complete the Human Subject 研究 CITI Program training course if you have not already. (你会发现注册说明 & 负责任行为的培训细节 的研究 这里)
3. 填写IRB申请表格 在这里 
   1. 尽你所能填写IRB申请表. 确保你 附上与你的项目有关的所有文件.g.，调查或问卷，同意 forms, flyers or advertisements used to solicit participants, CITI Program training 证书等.).
4. 将所有问题提交给IRB管理员 irb@r2painrelief.com.

Upon receiving your Application Form and attachments, the IRB Administrator will perform an initial review of your 项目 to determine what level of IRB review is appropriate.

人类受试者研究 Projects requiring a meeting of the full Institutional Review 董事会应尽快申请.

内部审查委员会在每个月的第一个星期五开会一次.

你可能会被要求向董事会提供更多的信息 before it decides to 批准或不批准你的项目. Please be aware that you cannot start your 项目 until you have the signed Approval 表格从完整的IRB.

皇冠博彩app的IRB管理员审查 所有 人类受试者研究- including classroom or practicum 项目s that will not be 发表. 请填写IRB申请表格.

• 你的项目可能有资格获得 Administrative Review, which will only take 很短的时间.
• Please be aware that you cannot start your 项目 until you have the signed Approval Form.

Students involved in research at NM Tech must 完整的 their CITI training in order 参与. This is to ensure a strong understanding of responsible and ethical research practices 项目设计. 学员应完成以下培训: 

• 负责任研究行为(RCR)课程
  • NMT学生/博士后
• 人文学科研究课程
  • NMT学生/博士后

If your research 项目 will NOT collect any Person所有y Identifiable Data from your 参与者:

• 你的项目可能有资格 管理的决心 为免.
• Please be aware that you cannot start your 项目 until you have the signed Approval 表格在手.

If your research 项目 WILL collect certain types of Person所有y Identifiable Data 参与者:

• 你的项目可能有资格获得 加快审查, which is performed by the IRB Administrator and one other IRB member. 这需要 up to three weeks to 完整的, depending on the availability of board members.
• Please be aware that you cannot start your 项目 until you have the signed Approval Form. 

您的项目可能需要全面审查.

This will require a meeting of the full Institutional Review Board, which can take 最多1个月的时间安排. 你可能会被要求向董事会提供更多的信息 在决定批准或不批准你的项目之前. Please be aware that you cannot start your 项目 until you have the signed Approval 表格从完整的IRB.

Person所有y Identifiable Data is defined by federal regulation as the following information:

• 名字 (i.e.、调查问卷上的姓名)
• 身份证号码 (i.e.(社会安全号码，理工学院学生证号码)
• 联系信息 (i.e., Physical Address, Phone Number, Email Address and/or IP Address) Audiotape recordings, videotape recordings, or photographic images of participants
• 参与者的血液、组织、体液或DNA
• 敏感的健康或医疗信息 (i.e., HIV status; drug/alcohol use; mental/physical disorders; illicit or criminal behaviors; or other information that could cause harm to the participant if it became 在他们的社区中众所周知.

您是否需要修改原始IRB的某些部分 批准 项目/research you will need to 完整的 the IRB修改表格. 以下 以下是你需要修改的原因:

• 申请临时IRB研究截止日期延期

OR

• 对以下内容进行更改:
  • 研究人员
  • 使用的研究程序
  • 知情同意文件
  • 参与研究的人类受试者类型
  • 收集的数据类型

Multi-year 项目s are initi所有y approved by the IRB for a 12-month period, any research expected to extend beyond that date must file yearly to renew the IRB 批准. PI负责不允许他们的IRB批准失效. 建议提交续期申请 60天或2个月 在过期日期之前. 

续期必须包括:

• A list of any changes proposed to the following areas of the original 批准 项目/research:
  • 研究人员
  • 使用的研究程序
  • 知情同意文件
  • 参与研究的人类受试者类型
  • 收集的数据类型
  • The IRB also asks that you provide a written explanation for these changes.
• 年度进度报告
  • The report should detail your 项目/research such as your progress/setbacks/breakthroughs/etc. so the IRB can quickly assess the work and avoid delaying your 批准 renewal.

Use this form to report unanticipated events or problems caused by or related to a 人类受试者参与您的研究项目. 

• 此后，不良事件极不可能发生 NMT不进行任何类型的临床研究，但我们根据联邦法律的要求提供此表格.