ACRP CCRC EXAM PREP 2024 QUESTIONS WITH COMPLETE ANSWERS GRADED A+

Adverse Drug Reaction (ADR) - CORRECT ANSWER In the pre-approval clinical experience with a new medicinal product or its new usages, particularly as the therapeutic dose(s) may not be established: all noxious and unintended responses to a medicinal product related to any dose should be considered adverse drug reactions. Adverse Event (AE) - CORRECT ANSWER Any untoward medical occurrence in a patient or clinical investigation subject administered a pharmaceutical product and which ...

Adverse Drug Reaction (ADR) In the pre-approval clinical experience with a new medicinal product or its new usages, particularly as the therapeutic dose(s) may not be established: all noxious and unintended responses to a medicinal product related to any dose should be considered adverse drug reactions. Adverse Event (AE) Any untoward medical occurrence in a patient or clinical investigation subject administered a pharmaceutical product and which does not necessarily have a causal relat...

LAR Legally Authorized Representative Essential documents documents which individually and collectively permit evaluation of the conduct of a study and quality of the data produced Who developed the Declaration of Helsinky? the World Medical Association Phase 1 study designed to determine the metabolic and pharmacologic action of the drug in humans monitor ultimately responsible for source data verification investigator leader of the research team who is ...

A subject is issued 120 tablets and is instructed to take 2 tablets 4 times a day. He returns 88 tablets on the morning of day 9 fasting for laboratory tests. What percent compliant is he? 50% To be eligible for a trial, the subjects must have liver function tests no greater than two times the upper limit normal and rental function tests no greater than three times the upper limit normal. All of the following are normal ranges for the trial: AST 5-65 ALT 5-35 BUN 4-25 Creat 0.5-1.2 ...

ADR Adverse Drug Reaction AE Adverse Event ALCOAC Accurate, Legible, Contemporaneous, Original, Attributable, and Complete ALT Alanine Transaminase (liver enzyme) AST Aspartate Transaminase (liver enzyme) BID Twice a day BMI Body Mass Index BP Blood Pressure BUN Blood Urea Nitrogen (kidney function test) C Celsius CAPA Corrective and Preventive Action CIOMS Council for International Organizations of Medical ...

Crossover when each subject is randomized to a sequence of two or more treatments and hence acts as their own control for treatment comparisons Parallel when subjects are randomized to 1 of 2 or more arms, each arm being allocated a different treatment. Each treatment will include their investigational product at one or more doses, and one or more control treatments, such as placebo and/or an active comparator A sponsor is developing an IP for treatment of a medical condition whe...

1571 IND application; Permit to do research on humans for the first time; has background info; and rationale; updated annually 1572 Investigator statement; commitment, done nationally and internationally by sponsors intending to hava marketing aproval for IP IB Clinical and non-clinical data on the investigational product that is relevant to the study in human subjects; supplied prior to regulatory approval Study type - Open Label everyone knows the treatment Stud...

Belmont Report (1979) ethical principles and guidelines for the protection of human subjects of research. respect for persons individuals should be treated as autonomous agents and persons with diminished autonomy are entitled to protection An autonomous person A person capable of deliberation about personal goals and of acting under the direction of such deliberation Beneficence Do not harm and maximize possible benefits and minimize possible harms Justice 1) to...

Adverse Drug Reaction (ADR) All noxious and unintended responses to a medicinal product related to any dose (causal relationship is at least a reasonable possibility). Regarding marketed medicinal products: a response to a drug which is noxious and unintended and which occurs at doses normally used in man for prophylaxis, diagnosis, or therapy of diseases or for modification of physiological function Adverse Event (AE) Any untoward medical occurrence in a patient or clinical investigati...