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 ...

Institutional Biosafety Committee – recombinant DNA, materials of human or non-human primate origin, toxins, select agents, etc. Radiation Safety Committee – radioactive materials Institutional Review ...

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 ...

If the information collected by your project is to be kept in house (i.e. not to be shared with the public) or collected for pedagogical reasons,( i.e., teaching purposes), it is not considered ...

Investigators must use Cayuse to electronically submit new research studies for review and approval, course approvals, continuing research requests, amendments to approved research studies, and ...

A single IRB (sIRB) of record will be used in the ethical review of non-exempt human subjects research protocols funded by federal agencies that are carried out at more than one site in the United ...

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 ...

NEW YORK & SALT LAKE CITY--(BUSINESS WIRE)--Protocol First, a software solutions provider focused on accelerating clinical research, has joined Flatiron Health Ⓡ as a wholly owned subsidiary, the two ...