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:

Weekly Updates: If you would like to be notified when new challenges become available please click here

Have you tried The Ultimate GCP Challenge Game?...... click here for more information

Number of Challenges & Tests Taken to date: 843,476

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

Quiz Title ( Guidelines )
Average Score
User Rating
Rating
ICH E Numbers
56%
3.1
ICH GCP Responsibilities
67%
3.7
ICH E17 - MRCTs
62%
3.8
ICH GCP (R2) Monitoring
68%
2.9
ICH GCP R2 Missing Words
56%
3.1
ICH GCP - Who am I?
65%
3.2
The letter N
54%
3.2
The Investigator
65%
3.4
AxMPs
62%
2.9
ICHE6
71%
2.9
Informed Consent
66%
3.2
Which document am I?
70%
3.6
Ensuring Quality
77%
3.6
ICH GCP Random questions
71%
3.5
ICH E8
69%
3.6
Electronic Informed Consent
76%
3.6
Updated ICH GCP and Related Guidelines
57%
3.1
ICH GCP R2
61%
3.2
ICH GCP Monitoring - Missing words
62%
2.8
General Considerations for Clinical Trials
53%
3.2
Document Control
67%
2.7
E Numbers
62%
2.2
ICH GCP - Monitoring
71%
3.2
Principles of ICH GCP
64%
3.4
Audits and Inspections
68%
3
ICH GCP - A selection of questions
66%
3
Adverse Events - ICH E2A
71%
3.2
Legal and Financial Responsibility
64%
2.9
Alternative Guidelines
51%
2.7
GCP Numbers
73%
2.9
21 CFR part 50
59%
3.1
ICH GCP Random questions
59%
2.6
ICH E3 Structure and Content of Clinical Study Reports
51%
2.6
ICH GCP Draft Addendum 2015
71%
3.1
21 CFR part 11 - Electronic Records and Electronic signatures
63%
2.9
ICH E2F - DSUR
55%
3.1
Specific Informed Consent Related Area
55%
2.6
ICH E11 - Clinical trials in children
61%
2.8
FDA forms
64%
3
Guideline Updates and Additions
51%
2.5
ICH GCP Words and Terms
48%
2.3
ICH GCP 10
62%
2.7
Electronic records and signatures - 21CFR part 11
66%
3.1
Guidelines, Legislation and Regulation
69%
2.8
EMA policy on publication of clinical data
55%
3
ICH GCP - missing words
62%
2.9
ICH GCP and the Protocol
52%
2.6
Placebo Controlled Trials
64%
2.9
GCP by Numbers
49%
2.7
Clinical Trials in the US
56%
3
Clinical Trials and GMP
54%
2.9
ICH E6 GCP Addendum
52%
2.5
Clinical Trials in Paediatrics - ICH E11
69%
3.4
ICH Defnitions
44%
2.6
GCP Revision
66%
2.9
ICH GCP - Who am I?
55%
2.7
Informed Consent - case studies
57%
3
ICH GCP - What am I?
66%
2.7
Does ICH GCP Say?
69%
3.2
ICH GCP and the Investigator
63%
2.7
ICH GCP essential documents
60%
2.6
ICH GCP Committees
57%
2.7
ICH GCP Odd One Out
52%
2.6
General ICH GCP
58%
2.3
Managing IMP
75%
3.2
ICH E9 for Everybody
48%
3.1
How Much Do You Know About Clinical Research Part 3: Guidelines and Regulations
60%
2.9
The GCP Challenge of 2013
65%
3.2
ICH GCP Definitions
61%
2.8
Declaration of Helsinki 2013
54%
2.8
International Conference on Harmonisation
63%
3.3
ICH GCP True or False II
69%
3.2
Geographical GCP
58%
3.1
ICH GCP - Who am I?
69%
3.1
ICH GCP Review
75%
3
ICH GCP Firsts
64%
2.5
ICH GCP Study Closeout
66%
2.7
Reporting clinical trials
55%
2.8
Do I know my ICH?
62%
3
ICH GCP Investigational Products
70%
2.9
ICH GCP Investigational Product
49%
2.4
FDA Inspections
57%
3.3
Informed Consent in ICH GCP
60%
2.4
Declaration of Helsinki
60%
2.7
ICH GCP - Principles
66%
2.4
General ICH GCP
56%
2.6
Ordering GCP
59%
2.3
ICH GCP Data Handling and Management
56%
3
ICH GCP - Descriptions
67%
2.7
ICH GCP - Trial Start Up
56%
2.7
ICH GCP True or False
70%
2.6
ICH GCP: Can you do better?
65%
3.1
ICH GCP - Monitoring
65%
2.3
ICH GCP Definitions
70%
2.6
GCP - EU vs USA
49%
2.8
E-GCP
71%
2.9
Understanding Endpoints
52%
2.3
Informed Consent Documents
45%
2.3
Do you know your ICH GCP?
68%
2.4
ICH GCP - The purpose of..
69%
3.2
International Clinical Trials Day 2013: Ultimate GCP Test
68%
2.8
ICH GCP Study Start-up
57%
3
Keeping ICH in Order
53%
2.2
Principles of ICH GCP
71%
3.9
ICH on Pharmacogenomics and Pharmacogenetics
53%
3.1
2012 GCP Test
56%
2.8
ICH GCP - random questions
59%
2.1
ICH GCP - The Investigators Brochure
78%
2.4
GCP Question Selection
65%
2.8
ICH Guidelines and Trial Design
51%
2.7
ICH GCP Test
65%
2.5
ICH GCP Informed Consent
91%
2.5
Clinical Trials in Africa
46%
3
ICH GCP Test
48%
2.5
Recruitment and Consent
61%
2.2
1, 2, 3, 4, 5 ....... ICH
55%
2.1
ICH GCP - which essential document?
69%
3
21 CFR part 312
48%
3.9
ICH E2A - Safety First
46%
2.1
GCP in Asia
40%
2.5
ICH GCP Monitoring
65%
2.8
ICH GCP Records and Reports
57%
2.6
ICH Guideline E2F DSURs
48%
2.3
Choice of control for clinical trials - ICH E10
50%
2.7
April GCP Updates
50%
2
ICH GCP General Questions III
60%
2.7
ICH - Know Your Guidelines?
55%
2.8
ICH Pharmacovigilance
52%
2.9
ICH GCP - Filing Essential Documents
59%
2.7
ICH - General Considerations for Clinical Trials
60%
3.2
ICH GCP - Training
61%
1.8
Informed Consent
53%
2
Guidelines for?
58%
2.6
ICH GCP - Does it say....?
67%
3.2
Serious Breaches
53%
3.3
GCP Hardest Ten of 2010
51%
3.2
IMPs in ICH GCP
56%
1.6
ICH GCP definitions
56%
2.4
GCP Combinations
58%
3.3
ICH GCP - Investigational Products
55%
2.5
ICH GCP General Questions II
62%
2.9
Clinical Study Reports
45%
1.4
Pharmacovigilance in clinical trials
49%
3
ICH GCP - Investigator responsibilities
55%
2.5
ICH GCP General Questions
60%
2.8
ICH Guidelines
47%
2.8
Clinical Trials Update 2009
35%
2.2
ICH GCP Monitoring
42%
2.8
ICH GCP - Investigator responsibilities
55%
2.5
FDA Regulations 2
61%
3.8
ICH GCP Definitions
66%
3.4
Investigational Medicinal Products
50%
2.8
GCP 2007
53%
3
ICH GCP Trial Master Files
60%
3.3
GCP Lists
52%
1
ICH GCP and the CRO
60%
2
ICH GCP Insurance and Indemnity
54%
1.7
ICH GCP - what do these have in common?
66%
2.5
ICH GCP Test
57%
2
ICH Trial Results Related Definitions
54%
1.5
Informed Consent - Subject Information
59%
2
Informed Consent - missing words
64%
2.5
GCP
56%
2.6
ICH GCP - Informed Consent
63%
2.4
ICH GCP - Investigator Qualifications and Agreements
54%
2.2
Ethics Committees (2)
52%
1.9
ICH E10 Choice Of Control Group
39%
2.7
ICH E16
54%
2.3
ICH GCP - Individual Roles
64%
2.1
IEC and IRBs
52%
2.1
ICH GCP General Questions IV
63%
3
FDA Guidance on the 1572 form
41%
3
ICH GCP 25 Question Test
49%
2.5
ICH - Adverse Events
54%
3.2
International GCP Guidelines
51%
2.8
ICH GCP IRB and IEC
51%
2.3
ICH GCP Multicentre Trials
54%
2.7
Clinical Research Forms
54%
2
GCP Compliance
57%
2.8
2008 version of Declaration of Helsinki
59%
2.5
ICH and GCP Numbers
62%
2.5
ICH GCP - Frequency of Terms
43%
3.1
ICH GCP - What is the Question?
51%
2.5
ICH GCP - The Protocol
60%
3.3
National Clinical Trial Guidelines
53%
2.8
General Considerations for Clinical Trials - ICH E8
54%
2.3
What is the purpose of....?
57%
2
ICH GCP - Section One
55%
2.4
ICH GCP Site Requirements
56%
2.6
Know your GCP
46%
2.2
What Does GCP Say?
51%
2.9
Ethics Committees in ICH GCP
54%
3
ICH GCP Audits
49%
2.3
ICH GCP - What is the difference?
62%
2.6
Subject Recruitment
66%
3.2
ICH GCP Informed Consent Section
63%
2.8
GCP 2008
40%
3
Sections of ICH GCP
47%
1.5
Ultimate GCP II
61%
3
Declaration of Helsinki
57%
3.1
GCP - Who am I?
67%
2
European Clinical Trials Legislation
44%
2.4
ICH GCP - Records and Reports
59%
2
ICH GCP - CRO and Sponsor
52%
2.4
GCP Definitions
62%
3.2
ICH GCP - who is responsible?
61%
2.8
ICH GCP - What am I?
47%
3.2
ICH GCP - Sponsor Responsibilities
60%
2.2
GCP What is Missing?
56%
3.4
Clinical Trials in India
52%
3
IMP labelling
47%
2.8
Informed Consent - Missing Words
61%
1.7
GCP.......What Next?
39%
1.9
Sum GCP!
52%
3
ICH GCP Audits
51%
2.5
General ICH GCP Questions
61%
2.4
GMP for IMP 4
42%
2.8
New UK Legislation
49%
2.5
ICH GCP Section 6
45%
2.3
ICH GCP - Section 5 The Sponsor
63%
2.4
ICH GCP - Which document?
61%
3.6
Principles of ICH GCP
62%
3.1
GCP - where in the world?
48%
2.2
Hardest GCP Related Questions
57%
3
GCP Essential Documents 2
55%
3
GCP - New EU requirements
49%
3.3
ICH GCP
67%
3.1
ICH GCP Missing Words
57%
3.1
FDA Regulations
64%
3.4
ICH GCP: RESEARCH
53%
3.2
ICH GCP: CLINICAL
66%
3.3
Informed Consent (2)
48%
2.8
ICH GCP missing words 2
71%
2.8
ICH Missing Words (2)
58%
2.6
ICH Missing Words
52%
3.1
GMP for IMP 3
49%
3.5
Ethics Committees
58%
3.1
Informed Consent
74%
2.8
GMP for IMP 2
51%
3.1
ICH Guidelines
58%
3
Essential Documents
64%
2.9
GMP for IMP
54%
3.2
EU Directives
48%
2.5
GCP Test
70%
2.8

Register for My GCP Zone

If you have a LMC Account or a MY GCP Zone Account click here to login

If you would like to record your scores for the various challenges and tests, collect CPD/CEU points and download certificates then you can register for a Free My GCP Zone Account below:

Complete the form below to register for My GCP Zone.
First Name:
Surname:
Country
Email:
Re-enter email:
Password:
Re-enter Password:
Your sector
Your job role
 
 

 

PharmaSchool Logins

Learning Management Centre
CPMC Login
My GCP Zone Login
Retrieve Online Order

Free GCP & Regulatory Updates

PharmaSchool Online Courses:
Click here for the full range of Online GCP, Clinical Research and Development Courses from PharmaSchool.
Users in the following countries:
ALBANIA ANDORRA ANGOLA ARGENTINA ARMENIA AUSTRALIA AUSTRIA AZERBAIJAN BAHRAIN BANGLADESH BARBADOS BELARUS BELGIUM BELIZE BENIN BERMUDA BHUTAN BOSNIA AND HERZEGOVINA BOTSWANA BRAZIL BRUNEI DARUSSALAM BULGARIA BURKINA FASO BURUNDI CAMEROON CANADA CHILE CHINA COLOMBIA CROATIA CZECH REPUBLIC DENMARK DOMINICAN REPUBLIC ECUADOR EGYPT ETHIOPIA FINLAND FRANCE GAMBIA GEORGIA GERMANY GHANA GREECE HAITI HONDURAS HONG KONG HUNGARY ICELAND INDIA INDONESIA IRAN, ISLAMIC REPUBLIC OF IRELAND ISRAEL ITALY JAPAN JORDAN KENYA KUWAIT LEBANON LITHUANIA LUXEMBOURG MACEDONIA, THE FORMER YUGOSLAV REPUBLIC OF MALAWI MALAYSIA MALI MEXICO MOLDOVA, REPUBLIC OF NEPAL NETHERLANDS NEW ZEALAND NIGERIA NORWAY PAKISTAN PANAMA PERU PHILIPPINES POLAND PORTUGAL PUERTO RICO QATAR ROMANIA RUSSIAN FEDERATION RWANDA SAO TOME AND PRINCIPE SAUDI ARABIA SENEGAL SERBIA SINGAPORE SLOVAKIA SLOVENIA SOUTH AFRICA SPAIN SRI LANKA SUDAN SWEDEN SWITZERLAND TAIWAN, PROVINCE OF CHINA TANZANIA, UNITED REPUBLIC OF THAILAND TURKEY UKRAINE UNITED ARAB EMIRATES UNITED KINGDOM UNITED STATES UZBEKISTAN VANUATU VIET NAM ZAMBIA ZIMBABWE
 
 
Courses
Resources
Other Services
News & Corporate Information