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Number of Challenges & Tests Taken to date: 912,142

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%	3
ICH GCP Responsibilities	63%	3.2
ICH E17 - MRCTs	62%	3.4
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%	3
The Investigator	64%	3
AxMPs	62%	2.9
ICHE6	70%	2.8
Informed Consent	63%	2.8
Which document am I?	67%	3.3
Ensuring Quality	75%	3.4
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	62%	2.7
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	69%	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	67%	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	52%	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?	54%	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%	2.3
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	51%	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....?	66%	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%	2.7
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%	2.7
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	54%	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%	2.7
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	58%	2.9
Essential Documents	64%	2.7
GMP for IMP	54%	2.9
EU Directives	48%	2.4
GCP Test	69%	2.8

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