ACRP - CCRC Exam

This class was created by Brainscape user Patrick Campbell. Visit their profile to learn more about the creator.

Decks in this class (14)

Declaration of Helsinki
Declaration of helsinki was first...,
Declaration of helsinki created,
When do research studies have to ...
8  cards
ICH Abbreviations - and definitions
Adr,
Ae,
Alt
100  cards
ICH E2A Definitions and Standards for Expedited Reporting
University of Cali slideshow
31  cards
ICH E6 Good Clinical Practice
Purpose of gcp,
What does gcp provide,
Irb responsibilities
148  cards
ICH E8 General Considerations for Clinical Trials
1. Considerations for development plan 2. Basic trial design 3. Stages of drug development
58  cards
E9 Statistical Principles
Double blind,
Crossover study,
Pros of crossover study design
86  cards
ACRP Exam Prep questions
Are the terms serious and severe ...,
Which of the following options de...,
Subject 3826 had to stay in the h...
141  cards
ICH Questions Part 1
In ich gcp an audit is defined as...,
In ich gcp an inspection is defin...,
In ich gcp monitoring is defined ...
22  cards
ICH Questions Part 2
According to ich the investigator...,
According to ich the sponsor may ...,
According to ich the investigator...
31  cards
ICH Questions Part 3
Regarding withdrawals or drop out...,
Ich guidelines for trial design i...,
Ich guidelines for protocol prepa...
28  cards
ICH Questions Part 4
Double blind study design entails...,
In a single blind trial the perso...,
The purpose of a double blind des...
27  cards
ICH Questions Part 5
With regard to liability claims t...,
The sponsor should ensure that in...,
With regard to access to medical ...
32  cards
Clinical Safety Data Management
An adverse event is defined as on...,
A subject in an arthritis clinica...,
A response to a medical product m...
26  cards
Exam Review
It is the 1 ____________ responsi...,
What determines requirements or s...,
Who is ultimately responsible for...
47  cards

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ACRP - CCRC Exam

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