Dr. Jones is participating in a clinical trial sponsored by ABBA Device Company. Dr. Jones submitted the required documents for IRB/EC approval, and the IRB/EC required significant changes to the consent document. Dr. Jones should:

Dr. Jones is participating in a clinical trial sponsored by ABBA Device Company. Dr. Jones submitted the required documents for IRB/EC approval, and the IRB/EC required significant changes to the consent document. Dr. Jones should: "Give notice to the sponsor of the IRB's requirements before using the revised consent document" What is a Consent document?A report including critical information concerning a medical operation or therapy, a clinical study, or genetic testing.It also contains information on potential hazards and advantages. If a person wishes to participate in the therapy, procedure, trial, or testing, he or she must sign the permission form.Learn more about Consent Document:https://brainly.com/question/28721127#SPJ1