If you are still unsure whether your project requires IRB approval, please do not hesitate to contact the HRPP office. To submit a human subjects research (IRB) ... (recruitment flyers, consent forms, ...

IRB review and approval is required before implementing any new recruitment procedures (advertisements, flyers, etc); changes to the consent process or forms; research methods, procedures, apparatus, ...

If you are still unsure whether your project requires IRB approval, please do not hesitate to contact the HRPP office. To submit a human subjects research (IRB) application, compile the information ...

The RePOSA study consists of two component studies. A four-week Phase 2 dose ranging trial that will determine the optimal dose of IHL-42X based on safety and efficacy in OSA patients, and a 52 ...

Regulatory steps completed with the competent authority (FDA) and institutional review board (IRB) approval received in the United States to commence TACTI-003 Patient recruitment into the trial ...

Patient recruitment for the study is now set to begin immediately. This milestone follows the successful IRB approval, pilot testing and evaluation of Nexalin’s Halo technology at UCSD.

Patient recruitment for the study is now set to begin immediately. This milestone follows the successful IRB approval, pilot testing and evaluation of Nexalin's Halo technology at UCSD. The study will ...