PharmaSchool GCP Challenges

There are over 350 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 My GCP Zone Account by clicking here:

Number of Challenges & Tests Taken to date: 917,985

GCP & Guidelines | Trial Design | Adverse Events | Monitoring | Statistics | Abbreviations | General | Show All

Quiz Title ( Guidelines )
Average Score
User Rating
Rating
GCP by Numbers
45%
2.3
ICH E Numbers
56%
2.9
ICH GCP Responsibilities
63%
3.2
ICH E17 - MRCTs
62%
3.3
ICH GCP (R2) Monitoring
65%
2.7
ICH GCP R2 Missing Words
57%
2.6
ICH GCP - Who am I?
63%
2.6
The letter N
56%
2.9
The Investigator
64%
2.9
AxMPs
62%
2.8
ICHE6
70%
2.8
Informed Consent
63%
2.8
Which document am I?
67%
3.3
Ensuring Quality
75%
3.3
ICH GCP Random questions
69%
3.3
ICH E8
68%
3.3
Electronic Informed Consent
73%
3.5
Updated ICH GCP and Related Guidelines
57%
2.9
ICH GCP R2
60%
3.1
ICH GCP Monitoring - Missing words
63%
2.8
General Considerations for Clinical Trials
53%
3.1
Document Control
66%
2.7
E Numbers
61%
2.1
ICH GCP - Monitoring
71%
3.1
Principles of ICH GCP
63%
3.3
Audits and Inspections
67%
2.9
ICH GCP - A selection of questions
65%
3
Adverse Events - ICH E2A
70%
3.1
Legal and Financial Responsibility
64%
2.9
Alternative Guidelines
51%
2.6
GCP Numbers
73%
2.8
21 CFR part 50
59%
2.9
ICH GCP Random questions
59%
2.5
ICH E3 Structure and Content of Clinical Study Reports
50%
2.6
ICH GCP Draft Addendum 2015
69%
3
21 CFR part 11 - Electronic Records and Electronic signatures
63%
2.9
ICH E2F - DSUR
54%
3
Specific Informed Consent Related Area
55%
2.6
ICH E11 - Clinical trials in children
61%
2.7
FDA forms
63%
2.9
Guideline Updates and Additions
51%
2.4
ICH GCP Words and Terms
48%
2.3
ICH GCP 10
61%
2.7
Electronic records and signatures - 21CFR part 11
65%
3.1
Guidelines, Legislation and Regulation
66%
2.7
EMA policy on publication of clinical data
54%
3
ICH GCP - missing words
62%
2.9
ICH GCP and the Protocol
51%
2.6
Placebo Controlled Trials
63%
2.9
Clinical Trials in the US
55%
2.9
Clinical Trials and GMP
51%
2.9
ICH E6 GCP Addendum
51%
2.5
Clinical Trials in Paediatrics - ICH E11
67%
3.3
ICH Defnitions
44%
2.5
GCP Revision
65%
2.9
ICH GCP - Who am I?
55%
2.6
Informed Consent - case studies
57%
3
ICH GCP - What am I?
65%
2.6
Does ICH GCP Say?
69%
3.2
ICH GCP and the Investigator
62%
2.6
ICH GCP essential documents
59%
2.6
ICH GCP Committees
56%
2.7
ICH GCP Odd One Out
52%
2.6
General ICH GCP
58%
2.3
Managing IMP
74%
3.2
ICH E9 for Everybody
48%
3.1
How Much Do You Know About Clinical Research Part 3: Guidelines and Regulations
59%
2.9
The GCP Challenge of 2013
65%
3.2
ICH GCP Definitions
60%
2.8
Declaration of Helsinki 2013
53%
2.8
International Conference on Harmonisation
62%
3.3
ICH GCP True or False II
68%
3.2
Geographical GCP
57%
3.1
ICH GCP - Who am I?
69%
3
ICH GCP Review
74%
3
ICH GCP Firsts
63%
2.4
ICH GCP Study Closeout
66%
2.7
Reporting clinical trials
54%
2.7
Do I know my ICH?
61%
2.9
ICH GCP Investigational Products
69%
2.8
ICH GCP Investigational Product
48%
2.3
FDA Inspections
56%
3.3
Informed Consent in ICH GCP
60%
2.4
Declaration of Helsinki
59%
2.6
ICH GCP - Principles
66%
2.3
General ICH GCP
56%
2.6
Ordering GCP
59%
2.1
ICH GCP Data Handling and Management
56%
3
ICH GCP - Descriptions
66%
2.5
ICH GCP - Trial Start Up
56%
2.7
ICH GCP True or False
69%
2.4
ICH GCP: Can you do better?
65%
3
ICH GCP - Monitoring
65%
2.3
ICH GCP Definitions
70%
2.6
GCP - EU vs USA
49%
2.8
E-GCP
70%
2.8
Understanding Endpoints
52%
2.1
Informed Consent Documents
44%
2.2
Do you know your ICH GCP?
67%
2.4
ICH GCP - The purpose of..
68%
3.1
International Clinical Trials Day 2013: Ultimate GCP Test
67%
2.8
ICH GCP Study Start-up
57%
2.9
Keeping ICH in Order
52%
2
Principles of ICH GCP
71%
3.7
ICH on Pharmacogenomics and Pharmacogenetics
52%
2.8
2012 GCP Test
57%
2.8
ICH GCP - random questions
58%
2.2
ICH GCP - The Investigators Brochure
77%
2.5
GCP Question Selection
65%
2.8
ICH Guidelines and Trial Design
51%
2.8
ICH GCP Test
64%
2.5
ICH GCP Informed Consent
90%
2.3
Clinical Trials in Africa
45%
2.7
ICH GCP Test
48%
2.3
Recruitment and Consent
59%
2
1, 2, 3, 4, 5 ....... ICH
54%
2.2
ICH GCP - which essential document?
68%
2.9
21 CFR part 312
48%
3.5
ICH E2A - Safety First
47%
2.2
GCP in Asia
40%
2.2
ICH GCP Monitoring
65%
2.7
ICH GCP Records and Reports
57%
2.4
ICH Guideline E2F DSURs
48%
1.6
Choice of control for clinical trials - ICH E10
50%
2.4
April GCP Updates
49%
2
ICH GCP General Questions III
59%
2.6
ICH - Know Your Guidelines?
55%
2.6
ICH Pharmacovigilance
52%
2.7
ICH GCP - Filing Essential Documents
59%
2.6
ICH - General Considerations for Clinical Trials
60%
3
ICH GCP - Training
60%
2
Informed Consent
52%
1.8
Guidelines for?
58%
2.2
ICH GCP - Does it say....?
67%
3
Serious Breaches
52%
3.2
GCP Hardest Ten of 2010
51%
3.1
IMPs in ICH GCP
56%
1.7
ICH GCP definitions
56%
2.3
GCP Combinations
58%
3.1
ICH GCP - Investigational Products
55%
2.4
ICH GCP General Questions II
62%
2.8
Clinical Study Reports
45%
1.3
Pharmacovigilance in clinical trials
49%
2.8
ICH GCP - Investigator responsibilities
56%
2.4
ICH GCP General Questions
60%
2.8
ICH Guidelines
47%
2.3
Clinical Trials Update 2009
34%
1.9
ICH GCP Monitoring
43%
2.6
ICH GCP - Investigator responsibilities
56%
2.4
FDA Regulations 2
61%
3.6
ICH GCP Definitions
66%
3.2
Investigational Medicinal Products
49%
2.7
GCP 2007
53%
2.4
ICH GCP Trial Master Files
60%
3.2
GCP Lists
52%
0.8
ICH GCP and the CRO
59%
1.8
ICH GCP Insurance and Indemnity
54%
1.8
ICH GCP - what do these have in common?
66%
2.4
ICH GCP Test
57%
2
ICH Trial Results Related Definitions
54%
1.2
Informed Consent - Subject Information
59%
1.8
Informed Consent - missing words
64%
2.4
GCP
56%
2.2
ICH GCP - Informed Consent
63%
2.3
ICH GCP - Investigator Qualifications and Agreements
54%
2.1
Ethics Committees (2)
51%
1.9
ICH E10 Choice Of Control Group
39%
2.3
ICH E16
54%
2
ICH GCP - Individual Roles
64%
1.9
IEC and IRBs
51%
1.9
ICH GCP General Questions IV
63%
2.7
FDA Guidance on the 1572 form
41%
2.7
ICH GCP 25 Question Test
48%
2.5
ICH - Adverse Events
54%
3
International GCP Guidelines
51%
2.2
ICH GCP IRB and IEC
51%
2.2
ICH GCP Multicentre Trials
54%
2.4
Clinical Research Forms
54%
1.7
GCP Compliance
57%
2.4
2008 version of Declaration of Helsinki
59%
2.3
ICH and GCP Numbers
62%
2
ICH GCP - Frequency of Terms
43%
2.8
ICH GCP - What is the Question?
51%
2
ICH GCP - The Protocol
60%
3.4
National Clinical Trial Guidelines
53%
2.2
General Considerations for Clinical Trials - ICH E8
55%
1.8
What is the purpose of....?
57%
2
ICH GCP - Section One
55%
2.2
ICH GCP Site Requirements
56%
2.4
Know your GCP
46%
1.8
What Does GCP Say?
51%
2.7
Ethics Committees in ICH GCP
54%
2.8
ICH GCP Audits
49%
2.3
ICH GCP - What is the difference?
62%
2.4
Subject Recruitment
65%
1.8
ICH GCP Informed Consent Section
63%
2.3
GCP 2008
40%
2.5
Sections of ICH GCP
47%
1.4
Ultimate GCP II
61%
2.6
Declaration of Helsinki
56%
3
GCP - Who am I?
67%
1.8
European Clinical Trials Legislation
44%
2.4
ICH GCP - Records and Reports
59%
1.8
ICH GCP - CRO and Sponsor
53%
2.4
GCP Definitions
62%
2.6
ICH GCP - who is responsible?
61%
2.6
ICH GCP - What am I?
47%
2.9
ICH GCP - Sponsor Responsibilities
60%
2.3
GCP What is Missing?
55%
3
Clinical Trials in India
51%
2.9
IMP labelling
47%
2.2
Informed Consent - Missing Words
61%
1.6
GCP.......What Next?
39%
1.7
Sum GCP!
51%
2.1
ICH GCP Audits
51%
2.5
General ICH GCP Questions
61%
2.2
GMP for IMP 4
42%
2.2
New UK Legislation
48%
2.5
ICH GCP Section 6
46%
2.1
ICH GCP - Section 5 The Sponsor
64%
2.3
ICH GCP - Which document?
59%
3.2
Principles of ICH GCP
61%
2.6
GCP - where in the world?
47%
1.9
Hardest GCP Related Questions
57%
2.6
GCP Essential Documents 2
55%
2.7
GCP - New EU requirements
49%
3.4
ICH GCP
66%
2.9
ICH GCP Missing Words
57%
2.8
FDA Regulations
64%
3.3
ICH GCP: RESEARCH
51%
3
ICH GCP: CLINICAL
65%
3.2
Informed Consent (2)
48%
2.6
ICH GCP missing words 2
71%
2.6
ICH Missing Words (2)
58%
2.4
ICH Missing Words
52%
2.8
GMP for IMP 3
48%
3.2
Ethics Committees
58%
3
Informed Consent
74%
2.7
GMP for IMP 2
51%
2.8
ICH Guidelines
57%
2.9
Essential Documents
64%
2.7
GMP for IMP
54%
3
EU Directives
48%
2.4
GCP Test
69%
2.8

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