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"I recently discovered the site and I love the challenges. It is a great way to learn" NP, USA
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Weekly GCP Challenge

These are short challenges that cover a wide range of topics in GCP and Clinical Research. A new challenge is posted every week. If you would like to record your scores to the weekly challenges or be informed when new ones are available you can register for updates and a free games account at the left hand side of the screen.

Quiz Title (showing: Guidelines)
Average Score
International Clinical Trials Day 2013: Ultimate GCP Test
62%
ICH GCP Study Start-up
51%
ICH GCP Study Closeout
62%
Declaration of Helsinki
58%
Reporting clinical trials
56%
Keeping ICH in Order
49%
ICH GCP Test
65%
Do you know your ICH GCP?
68%
ICH GCP - The Investigators Brochure
77%
ICH GCP - The purpose of..
69%
FDA Inspections
56%
ICH on Pharmacogenomics and Pharmacogenetics
52%
Principles of ICH GCP
71%
1, 2, 3, 4, 5 ....... ICH
55%
ICH GCP Informed Consent
92%
ICH GCP - Training
62%
Understanding Endpoints
52%
GCP Question Selection
65%
ICH Guidelines and Trial Design
49%
Informed Consent
53%
2012 GCP Test
52%
ICH GCP - which essential document?
68%
E-GCP
70%
ICH GCP Definitions
68%
ICH GCP: Can you do better?
60%
21 CFR part 312
45%
Informed Consent in ICH GCP
57%
ICH GCP - Monitoring
62%
ICH E2A - Safety First
44%
ICH GCP - Principles
64%
Ordering GCP
54%
ICH GCP - Descriptions
64%
ICH GCP - Trial Start Up
53%
ICH GCP - random questions
56%
General ICH GCP
53%
Do I know my ICH?
58%
GCP - EU vs USA
46%
ICH GCP Investigational Products
66%
ICH GCP True or False
67%
ICH GCP Data Handling and Management
53%
Clinical Trials in Africa
43%
Guidelines for?
56%
GCP in Asia
39%
ICH GCP - Does it say....?
65%
Serious Breaches
50%
ICH GCP Monitoring
62%
ICH GCP Records and Reports
55%
ICH Guideline E2F DSURs
46%
April GCP Updates
48%
Choice of control for clinical trials - ICH E10
49%
ICH Pharmacovigilance
50%
GCP Lists
51%
ICH GCP and the CRO
59%
ICH GCP Insurance and Indemnity
52%
IMPs in ICH GCP
54%
GCP Hardest Ten of 2010
48%
ICH E10 Choice Of Control Group
36%
ICH GCP - Investigational Products
54%
ICH E16
52%
ICH GCP - what do these have in common?
65%
ICH GCP - Individual Roles
63%
IEC and IRBs
51%
ICH GCP General Questions IV
61%
ICH GCP General Questions III
58%
FDA Guidance on the 1572 form
39%
ICH GCP 25 Question Test
42%
ICH GCP General Questions II
61%
ICH - Know Your Guidelines?
53%
ICH - General Considerations for Clinical Trials
58%
ICH GCP General Questions
58%
International GCP Guidelines
50%
ICH GCP - Filing Essential Documents
56%
ICH GCP IRB and IEC
48%
Clinical Study Reports
43%
ICH GCP Multicentre Trials
51%
ICH GCP Test
57%
Clinical Research Forms
53%
ICH GCP - Frequency of Terms
41%
ICH GCP - What is the Question?
49%
ICH GCP - The Protocol
58%
ICH Trial Results Related Definitions
52%
ICH Guidelines
46%
Informed Consent - Subject Information
58%
Clinical Trials Update 2009
33%
National Clinical Trial Guidelines
51%
General Considerations for Clinical Trials - ICH E8
52%
What is the purpose of....?
56%
ICH GCP - Section One
53%
ICH GCP Site Requirements
54%
Know your GCP
44%
Informed Consent - missing words
63%
What Does GCP Say?
49%
Ethics Committees in ICH GCP
53%
ICH GCP - What is the difference?
62%
Subject Recruitment
65%
ICH GCP Informed Consent Section
62%
ICH GCP definitions
54%
GCP Combinations
56%
GCP Compliance
56%
GCP 2008
39%
Sections of ICH GCP
46%
2008 version of Declaration of Helsinki
58%
Ultimate GCP II
58%
Pharmacovigilance in clinical trials
48%
GCP
56%
Declaration of Helsinki
56%
GCP - Who am I?
66%
ICH GCP - Informed Consent
63%
ICH GCP - Investigator Qualifications and Agreements
51%
ICH GCP - Records and Reports
58%
ICH GCP - CRO and Sponsor
50%
GCP Definitions
61%
ICH GCP - who is responsible?
60%
ICH GCP - What am I?
45%
ICH GCP - Sponsor Responsibilities
58%
ICH GCP - Investigator responsibilities
52%
GCP What is Missing?
54%
Clinical Trials in India
51%
IMP labelling
46%
Informed Consent - Missing Words
60%
ICH GCP Audits
48%
GCP.......What Next?
38%
ICH GCP Monitoring
39%
Sum GCP!
49%
ICH GCP Section 6
43%
ICH GCP - Investigator responsibilities
52%
ICH - Adverse Events
53%
ICH GCP - Section 5 The Sponsor
52%
ICH GCP - Which document?
58%
Principles of ICH GCP
60%
GCP - where in the world?
46%
ICH and GCP Numbers
60%
FDA Regulations 2
57%
ICH GCP Definitions
63%
Hardest GCP Related Questions
54%
GCP Essential Documents 2
52%
GCP - New EU requirements
46%
ICH GCP
64%
Investigational Medicinal Products
48%
GCP 2007
50%
ICH GCP Trial Master Files
56%
ICH GCP Audits
48%
Ethics Committees (2)
50%
General ICH GCP Questions
59%
FDA Regulations
62%
ICH GCP: RESEARCH
50%
ICH GCP: CLINICAL
63%
GMP for IMP 4
39%
ICH GCP Missing Words
53%
Informed Consent (2)
47%
ICH GCP missing words 2
70%
European Clinical Trials Legislation
43%
ICH Missing Words (2)
55%
GMP for IMP 3
46%
New UK Legislation
48%
ICH Missing Words
50%
Ethics Committees
57%
Informed Consent
74%
GMP for IMP 2
49%
ICH Guidelines
51%
Essential Documents
62%
GMP for IMP
53%
EU Directives
46%
GCP Test
67%

 

 

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