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: 918,357

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	70%	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	63%	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	59%	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

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: Email: Re-enter email: Password: Re-enter Password: