The IRB will determine Whether the methods used for management ... A DSMP is sufficient for many types of studies, such as most Phase I and Phase II trials or investigator-initiated studies conducted ...
Your IRB Protocol number serves as both your SARC and IRB identifiers. To obtain your IRB Protocol number you will need to submit the Protocol Title and PI Information into the eRA website to generate ...
announced today the approval of an Investigational Review Board (IRB) sanctioned Phase II clinical study. The study (NCT06656351) will evaluate the efficacy and safety of the ARAKODA® regimen ...
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LEXX: IRB Approval Clears Way for GLP-1 Study #5Upon completion, the Phase Ib study is expected to be recognized ... Lexaria received independent review board (IRB) approval in January, clearing the way to begin its Human GLP-1 Study #5 ...
Following the completion of IRB initial training, UAB IRB policy requires refresher training once every three years for key personnel involved in human subjects research. All training courses are ...
EXCLUSIVE: MIRA Pharmaceuticals Kick Starts Human Trial In Israel For Ketamir-2 For Neuropathic Pain
On Tuesday, the Israeli Ministry of Health and the Institutional Review Board (IRB) approved MIRA Pharmaceuticals, Inc.'s (NASDAQ:MIRA) Phase 1 trial for Ketamir-2, the company's novel oral ketamine ...
All Wilkes University IRB Applications must be submitted through the IRB Mentor system. Applications will no longer be accepted by email. To access IRB Mentor, login through the Wilkes Portal. Then, ...
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