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CCRP

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

By: Dylan Drum
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Decks in this class (13)

The CITI Good Clinical Practice Course for Clinical Trials with Investigational Drugs and Medical Devices
On july 12 1974 the national rese...,
What was the national commission ...,
Four considerations for the natio...
44  cards
Overview of New Drug Development
0  cards
Overview of ICH GCP
Formed in the early 90s by repres...,
In what year did the internationa...,
What is the goal of the ich
42  cards
ICH-Comparison Between ICH GCP E6 and U.S. FDA Regulations
0  cards
Conducting Investigator-Initiated Studies According to FDA Regulations and GCP
0  cards
Investigator Obligations in FDA-Regulated Clinical Research
0  cards
Managing Investigational Agents According to GCP Requirements
0  cards
Overview of U.S. FDA Regulations for Medical Devices
0  cards
Informed Consent in Clinical Trials of Drugs, Biologics, and Devices
0  cards
Detecting and Evaluating Adverse Events
0  cards
Reporting Serious Adverse Events
0  cards
Monitoring of Clinical Trials by Industry Sponsors
0  cards
Audits and Inspections of Clinical Trials
0  cards

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CCRP

  • Class purpose General learning

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