CCRP EXAMS BUNDLE ~ Questions with 100% Correct Answers/Already Grade A+

21 CFR 11 - Electronic Records; Electronic Signatures B - Electronic Records C - Electronic Signatures 21 CFR 50 - Protection of Human Subjects/Informed Consent B - Informed Consent 50.23 - Exception from General 50.24 - Exception from Informed Consent Requirements for Emergency Research 50.2...

SAE - Serious Adverse Event: - results in death - is life threatening (patient was at risk of death at time of the event) - results in persistent or significant disability - congenital anomaly/birth defect Short Form - A document that states that the elements of informed consent have been pres...

Year/ description of the Nuremberg Code - 1947- German physicians conducted unethical experiments on concentration camp prisoners without their consent. What implications came of the Nuremberg Code? - Ten elements of human research including voluntary informed consent is absolutely essential. Ye...

How many days does a sponsor have to report an emergency use of an IP to the FDA? - 5 working days How many members must sit on an IRB? - 5 How long must an IRB retain records per 21 CFR 56? - 3 years after completion of research What are the criteria for IRB approval of research? (7) - 1. Risk...

Assessment - an objective evaluation or appraisal of an individual's health status, including acute and chronic conditions How does an assessment gather information? - through collection of data, observation, and physical examination What type of assessment? •Gather information about the pa...