Follow the step-by-step instructions below to successfully maintain and close a protocol with the IRB. Instructions below include information about continuing reviews, amendments, event reporting (new ...

Most pharmaceutical manufacturers utilize the gold standard of clinical trial design: randomized, controlled trials (RCTs) executed in four phases. Any protocols used must be approved by the FDA under ...

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 ...

A protocol deviation or violation is any departure from the study procedures or treatment plans as specified in the IRB-approved protocol. Protocol deviations occur when an investigator does not ...

Download the template(s) of your choice. The template documents open as Word files; save as a Word file to begin drafting your protocol. All instructions in the template are highlighted in blue.

The clinical research environment has undergone considerable transformation over the past decade. Protocols are more complex, product pipelines increasingly target smaller and more distributed patient ...

More processors on SoCs means more sophisticated cache control. This article describes formal techniques for verifying cache coherency for the ARM AMBA AXI Coherency Extensions (ACE) protocol. Fig 1.

This guidance provides directions for researchers using measures that involve questions related to suicidal ideation. Research shows that asking questions related to suicidal ideation (SI) does not ...

Effective April 21, 2021, all new protocols must be submitted using DragonSPOT. Please note the submission deadlines and the review processes will remain unchanged. IACUC Protocols are approved for a ...