The Lawrence Tech IRB (IRB00005791, expires 01/19/2025) is organized and operated according to guidelines of the United States Office for Human Research Protections and the United States Code of Federal Regulations and operates under Federal Wide Assurance No. FWA00010997, expires 09/29/2025.

The main responsibility of the 利记sbo IRB is to protect the rights and welfare of the human subjects participating in research conducted by representatives of Lawrence Tech (e.g., 教师, 工作人员, students) as well as monitoring research development, testing and evaluation methods. 

The 利记sbo IRB is co-chaired by Dr. 马修·科尔 , Interim Dean, College of Business and Information Technology, and Dr. 艾哈迈德Al-Bayati , Assistant Professor, College of 工程. The IRB is comprised of an interdisciplinary team of 教师 and 工作人员. The IRB is committed to maintaining the highest level of ethical standards to ensure protection of all human research participants. IRB approval is generally not required when human subjects data are used for "in-house" review, such as teaching evaluation, 课程评价, 或者质量保证. 

All human subjects research that is being conducted for grants and/or contracts requires IRB approval. IRB approval is also required if you plan on publishing the data beyond Lawrence Tech, such as in a conference presentation or journal publication. Please review the following flow chart on when 利记sbo IRB approval is required:  When is 利记sbo IRB Approval Required?  To begin the IRB approval process complete the 申请批准 to Conduct Research with Human Participants 并服从于 irb@femdomcenter.com prior to inviting any participants to your study. 

To protect yourself and act proactively with regards to helping the IRB comply with federal requirements please contact irb@femdomcenter.com 有问题吗?.

Except for internal departmental, 大学, 大学, or other Lawrence Tech administrative purposes, such as teaching evaluation, 课程评价, 或者质量保证, all requests to recruit Lawrence Tech 教师, 工作人员, and students for participation in research will be made to irb@femdomcenter.com and will be accompanied by the 申请批准 to Conduct Research with Human Participants .

IRB成员

Dr. 马修·科尔 , Associate Professor Management and Psychology, IRB Chair (Sole reviewer for Exempt and Expedited review paths)

Dr. David Svinarich, Vice President, Research/Academic Affairs, Ascension Michigan (External Member)

Dr. Therese贾米森 护理主任

Dr. 埃里克·迈耶 , Associate Professor Biomedical 工程

Dr. 朱莉Zweisler-Vollick , Associate Professor Biology and Biochemistry

凯瑟琳扳手 , Director of Sponsored Research & 机构资助

一般信息

教务长的IRB备忘录  

利记sbo Activites Requiring IRB Approval  

了解一切   IRB的介绍  Dr. 马修·科尔

Online Training Training Exam - Required for IRB Approval

Online Training Exam Study Guide  

Protecting Human Subjects Video - Part 1 ( National Institutes of Health )

Protecting Human Subjects Video - Part 2 ( National Institutes of Health )

Protecting Human Subjects Video - Part 3 ( National Institutes of Health )

IRB申请及表格

申请批准 to Conduct Research With Human Participants PDF

Informed Consent Form Template for BME Project 医生  

Informed Consent Form Template for Survey or Interview 医生  

Informed Consent Form Template for Online Survey 医生  

Template for Preparing a Participant Recruitment Flyer  医生  

Confidentiality Agreement Template 医生  

Data Use Agreement Template 医生  

申请批准 to Continue Research With Human Participants 医生  

If you have any questions about IRB processes, procedures, or forms, please contact irb@femdomcenter.com or  mcole@femdomcenter.com .

联系

Kathryn扳手,MBA, CRA
执行董事
Sponsored Research and 机构资助

E   kwrench@femdomcenter.com
P  248.204.3067
O  21415 Civic Center Drive, Suite 200, Building 18-South

建议书通知表格

利记sbo预算模板