using infectious agents with research participants the IBC protocol involves the use of human research participants or identifiable human biospecimens An IRB protocol submission is not required to the ...
Follow the step-by-step instructions below to successfully prepare and submit a protocol to the IRB. Instructions below include information about single IRBs, student involvement in human subject ...
Cal Lutheran investigators are expected to conduct human subjects research in an ethical manner in accordance with federal, state, and local regulations, institutional policy, and as described in the ...
Radiation Safety Committee – radioactive materials Institutional Review Board – use of human subjects Environmental ... Safety for further information and guidance. Your Animal Use Protocol has been ...
Projects/packages requiring Full Committee Review must be determined to be complete before these are placed on the agenda for review at a scheduled IRB meeting. Project/packages requiring ...
A thorough review of exempt research may be found here. What is an expedited protocol? Will it be approved more quickly? The IRB may use an expedited review procedure when the research involves no ...
BioLab Holdings, Inc., a Phoenix-based medical manufacturer specializing in wound healing and wound care products, is pleased to announce the approval of its randomized control trial designed to ...
You cannot use the laboratory if your IRB has expired! Please ensure your IRB protocol is consistent with the best practices from the BC/IRB perspective, especially with respect to data storage (see ...
A new study monitored smartphone data to understand screen time use by adolescents. The report, called "Adolescent Smartphone ...
All WMU IRB submissions must be completed using Cayuse, an online IRB protocol management system. Researchers may access Cayuse using their WMU Credentials. Note: Students are not automatically given ...
The Smith College Institutional Review Board (IRB) upholds the principles of respect, beneficence and justice, with established guidelines to ensure that human research participants are treated with ...