UConn Health has acknowledged that it had a lapse in an approved research protocol involving use of animals in the research process and that it was reported to federal regulators. A spokeswoman for ...

What if I told you that there was a plant that could be used to treat diabetes, liver problems, ulcers, leukemia, and malaria? Understandably, you would want that plant to be studied and turned into ...

Note that all forms must be completed on a computer. No handwritten forms will be accepted for review. Before you take the time to prepare your protocol, you want to make sure the project you are ...

The Initial Protocol Application, like all of the HRPP webforms, is an interactive form with built-in logic. That means that the answers to some questions will reveal other questions. Only the ...

The Post Approval Monitoring (PAM) team within Research Regulatory Affairs aims to help ensure the well-being of humans and vertebrate animals involved in research. Authorization for researchers to ...

The flowchart and steps below outlines the best practice for processing industry-written and sponsored clinical trials at UAB. There are many small steps in each of the larger defined steps (see flow ...

Researchers worldwide can now create highly realistic brain cortical organoids—essentially miniature artificial brains with functioning neural networks—thanks to a proprietary protocol released this ...

Jamjoom Pharma, a leading pharmaceutical company, and the Research Institute of Ophthalmology have signed a cooperation ...

The Principal Investigator (PI) is responsible for reviewing this policy and complying with its requirements. Specifically, the PI will: You may use the protocol template to record your information ...