[Answer] When must the investigator update the IRB about the progress of a trial?

Answer: during the conduct of the trial and at the termination

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When must the investigator update the IRB about the progress of a trial? 9 years . Adults with more than 12 months history of migraines were assigned randomly in a double-blinded study to receive treatment with experimental drug X or placebo. The primary efficacy measure was the reduction in the severity of the migraine attacks. The investigator must report adverse events to the: Sponsor. When must the investigator update the IRB about the progress of a trial ? During the conduct of the study and at termination. Which of the following is an investigator s commitment to the sponsor? Submit a … FDA requires Investigator to inform the subject's primary physician about the subject's participation in the trial if subject has a PCP and if the subject agrees to the primary physician being informed. When must the investigator update the IRB about the progress of a trial ? Conduct or supervise the investigation personally In completing Form FDA 1572 Statement of Investigator the investigator … When must the investigator update the IRB about the progress of a trial ? ... a subject participating in a trial MUST be paid. False. T or F: a sub-I and a Co-I are the same thing? ... (FDA definition) a co- Investigator is defined the same. What basic information should be documented in the progress notes concerning the Informed Consent Process ... When Must The Investigator Up...

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