Acrp ccrc study guide - Study guides, Class notes & Summaries

ACRP Key Terms for CCRC exam, CCRC Exam, ACRP CCRC EXAM PREP, CCRC Exam Prep, ACRP CCRC, *CCRC Study Set 3.4.21 LATEST UPDATE 2023|2024 GRADED A+ Human Pharmacology Study -Assess Tolerance -Define/Describe pharmacokinetics and pharmacodynamics -explore drug metabolism and drug interactions -estimate activity Human Pharmacology Study Examples: -dose tolerance studies -single and multiple does pharmacokinetics and pharmacodynamic studies -drug interaction studies Therapeutic Explorator...

CCRC Module 2: Overview of ACRP Certification Exam References Questions and Answers 2023 Regulations - are issued by regulatory authorities such as the FDA, or European Medicines Agency [EMA] -applicable only in the country or countries within the jurisdiction of these authorities (e.g. FDA = USA, EMA = Europe) The 3 primary ICH regions Japan, USA, EU Why did ICH guidelines develop? To prevent duplication of efforts in 3 countries [Japan, US, EU] when industry and regulatory...

ACRP CCRC Study Guide Exam Questions and Answers (235 Questions) All Correct

ACRP CCRC Study Guide questions and answers 2023

ACRP CCRC Study Guide Latest 2023 Graded A What is ICH E2A? Clinical Safety Data Management -Definitions and Standards for Expedited Reporting -This document gives standard definitions and terminology for key aspects of clinical safety reporting. -It also gives guidance on mechanisms for handling expedited (rapid) reporting of adverse drug reactions in the investigational phase of drug development. ICH E2A: An adverse event is defined as one which a) Results in hospitalization b) Causes a disa...

ACRP CCRC Exam Study Guide Solutions ADR - ANSWER-Adverse Drug Reaction Audit - ANSWER-Reviews how the research was conducted; takes into account SOPs, IRB requirements & GCP (ensures compliance) Audit Certificate - ANSWER-Confirmation audit took place Audit Report - ANSWER-Written Evaluation - not regularly made available to regulatory body; only when serious evidence exists concerning non-compliance Audit Trail - ANSWER-Documentation of audit events Single Blind Study - ANSWER-Subjects...

QUESTIONS AND ANSWERS

QUESTIONS AND ANSWERS