WebSupplemental Forms. Device Form: Used for any study involving medical devices (as defined by the FDA) Specimen Form: Used for any study collecting or using Human biological specimens for research (e.g., organ tissue, plasma, urine, feces, cells). This may include specimens collected as part of routine care for use as part of the research. WebAnimal work with DOD or ONR funding must be detailed in its own IACUC protocol. Please contact the ARC office at [email protected] for more information on these and other very detailed requirements. DO NOT SUBMIT DOCUMENTS DIRECTLY TO DOD/ONR/VA. The forms and requirements change often.
Protocol Submission Research Integrity and Assurance
WebApr 7, 2024 · Research Involving Animals The IRB reviews research that involves human participants. Research involving animals must be reviewed by the Institutional Animal … WebThe IRB is responsible for safeguarding the rights and welfare of human subjects involved in any IRB approved research related activity, and for assuring proper laboratory practices, … rabbits red eyes
Ethics in Research: What is the IRB? – ScIU
WebIn accordance with FDA regulations, an IRB has the authority to approve, require modifications in (to secure approval), or disapprove research. This group review serves … WebApr 7, 2024 · Institutional Animal Use and Care Committee, IACUC. Federal law mandates that all animal research with vertebrates be carefully reviewed by a panel of expert and … WebJan 15, 2024 · Animals in NIH Research Animal Welfare Application Submission Policies Clinical Trial Requirements Coronavirus Disease 2024 (COVID-19) Early Stage Investigator Policies Family-Friendly Initiatives Financial Conflict of Interest Foreign Interference Human Subjects Research Inclusion Policies rabbits reading