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Number of Challenges & Tests Taken to date: 908,848

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

Quiz Title ( All )	Average Score	User Rating	Rating
Industry Update	40%	0.8
GCP Lists	52%	0.8
International Clinical Trials	50%	1
Christmas GCP	54%	1
Clinical Systems and Software	39%	1
Sum More GCP	44%	1.1
The Letter C	68%	1.1
Approvals and Global Sales	46%	1.2
The letter G	60%	1.2
ICH Trial Results Related Definitions	54%	1.2
Clinical Study Reports	45%	1.3
Foreign Clinical Trials	70%	1.3
Sections of ICH GCP	47%	1.4
Clinical Pharmacology	62%	1.4
What's the difference?	57%	1.4
The Letter O	72%	1.4
Getting Products to Market	46%	1.4
Geographical GCP	42%	1.5
IRB vs IEC	49%	1.5
Where would you find...............?	47%	1.5
Laboratory Tests	70%	1.6
Interpreting Trial Results	41%	1.6
ICH Guideline E2F DSURs	48%	1.6
Famous Pharmaceutical Companies	54%	1.6
The Letter P	70%	1.6
Informed Consent - Missing Words	61%	1.6
Clinical Research All-Rounder II	46%	1.7
GCP.......What Next?	39%	1.7
What is?	52%	1.7
GCP Update 2010	52%	1.7
The International Conference on Harmonisation	45%	1.7
IMPs in ICH GCP	56%	1.7
Clinical Trials: What's the difference?	36%	1.7
Clinical Research Forms	54%	1.7
Clinical Trial Percentages	52%	1.8
Who am I?	34%	1.8
GCP Revision 2011 Half 1	37%	1.8
Informed Consent - Subject Information	59%	1.8
GCP - Who am I?	67%	1.8
GCP Inspections	46%	1.8
Proposed new EU legislation on Clinical Trials	47%	1.8
General Considerations for Clinical Trials - ICH E8	54%	1.8
Informed Consent	52%	1.8
Orphan Drugs	38%	1.8
Subject Recruitment	65%	1.8
ICH GCP - Records and Reports	59%	1.8
Clinical Research Definitions	63%	1.8
Sample Sizing for Clinical Researchers	58%	1.8
Odd one out	42%	1.8
Regulatory What Is It?	37%	1.8
Know your GCP	46%	1.8
ICH GCP Insurance and Indemnity	54%	1.8
Clinical Trials Update 2009	35%	1.9
Clinical Trial Permissions	41%	1.9
Regulatory Agencies	46%	1.9
Ethics Committees (2)	51%	1.9
Clinical Laboratory Tests 2	68%	1.9
GCP - where in the world?	47%	1.9
What's in a name?	42%	1.9
ICH GCP - Individual Roles	64%	1.9
ICH and GCP Numbers	62%	2
Regulatory - What is it? II	44%	2
ICH GCP and the CRO	59%	2
ICH E16	54%	2
April GCP Updates	49%	2
ICH GCP - What is the Question?	51%	2
International GCP Update	40%	2
IEC and IRBs	51%	2
What is the purpose of....?	57%	2
Health Economics in the UK	34%	2
GCP, Guides, Books and Colours	49%	2
Keeping ICH in Order	52%	2
ICH GCP - Training	60%	2
Who is responsible for?	53%	2
ICH GCP Test	57%	2
Recruitment and Consent	59%	2
ABC of Clinical Trials	58%	2.1
Clinical Trial Phases	49%	2.1
Hardest 20 of 2012	48%	2.1
Ordering GCP	59%	2.1
E Numbers	61%	2.1
ICH GCP - random questions	58%	2.1
Clinical Research - Things I Should Know	62%	2.1
Sum GCP!	51%	2.1
FDA - new regulation governing foreign clinical trials	43%	2.1
Understanding Endpoints	52%	2.1
ICH GCP - Investigator Qualifications and Agreements	54%	2.1
ICH GCP Section 6	46%	2.1
GCP in Asia	40%	2.2
ClinicalTrials.gov	39%	2.1
Medical Abbreviations	74%	2.2
Pharmaceuticals in Modern Culture	44%	2.2
Guidelines for?	58%	2.2
ICH GCP - Section One	55%	2.2
Welcome to 2013	48%	2.2
Drug Life Cycle Terms	53%	2.2
Clinical Trial Measurement Scales	46%	2.2
ICH E2A - Safety First	47%	2.2
International GCP Guidelines	51%	2.2
National Clinical Trial Guidelines	53%	2.2
GMP for IMP 4	42%	2.2
Clinical Trial Design 3	49%	2.2
IMP labelling	47%	2.2
GCP	56%	2.2
ICH GCP IRB and IEC	51%	2.2
25 Question GCP and CR Test	57%	2.2
Protocol Design	41%	2.2
General ICH GCP Questions	61%	2.2
Name the year	51%	2.2
1, 2, 3, 4, 5 ....... ICH	54%	2.2
GCP by Numbers	45%	2.3
Trial Design 2	54%	2.3
ICH GCP definitions	56%	2.3
ICH GCP Words and Terms	48%	2.3
Informed Consent Documents	44%	2.3
ICH GCP - Informed Consent	63%	2.3
ICH GCP Audits	49%	2.3
Clinical Trial Measurements	60%	2.3
ICH E10 Choice Of Control Group	39%	2.3
Statistics in Protocols	46%	2.3
Designs of Clinical Trials	47%	2.3
ICH GCP - Sponsor Responsibilities	60%	2.3
2008 version of Declaration of Helsinki	59%	2.3
Compassionate Use	47%	2.3
Numbers	47%	2.3
ICH GCP - Principles	66%	2.3
Randomisation	46%	2.3
ICH GCP - Section 5 The Sponsor	64%	2.3
ICH GCP Investigational Product	48%	2.3
General ICH GCP	58%	2.3
ICH GCP Test	48%	2.3
Analyses	49%	2.3
PharmaSchool Favourites	47%	2.3
ICH Guidelines	47%	2.3
ICH GCP - Monitoring	65%	2.3
ICH GCP Informed Consent Section	63%	2.3
The Letter T	60%	2.3
ICH GCP Informed Consent	90%	2.3
ICH GCP - CRO and Sponsor	53%	2.4
EU Directives	48%	2.4
ICH Missing Words (2)	58%	2.4
ICH GCP True or False	69%	2.4
ICH GCP - what do these have in common?	66%	2.4
Keeping Research in Order	45%	2.4
Early Phase Trials	55%	2.4
Guideline Updates and Additions	51%	2.4
Advanced Therapies	48%	2.4
Do you know your ICH GCP?	67%	2.4
ICH GCP Audits	51%	2.4
Pharma Industry	42%	2.4
GCP Compliance	57%	2.4
Legislation or Guidance?	71%	2.4
Product Types and Uses	66%	2.4
Informed Consent - missing words	64%	2.4
GCP 2007	53%	2.4
European Clinical Trials Legislation	44%	2.4
Health Economics	37%	2.4
ICH GCP Multicentre Trials	54%	2.4
Informed Consent in ICH GCP	60%	2.4
Seasonal Competition Quiz	42%	2.4
ICH GCP - Investigator responsibilities	56%	2.4
ICH GCP - Investigator responsibilities	56%	2.4
History of the FDA	45%	2.4
Choice of control for clinical trials - ICH E10	50%	2.4
ICH GCP - Informed Consent	56%	2.4
ICH GCP - What is the difference?	62%	2.4
Concomitant Medication	72%	2.4
More Abbreviations	68%	2.4
ICH GCP - Investigational Products	55%	2.4
Medications and Medication Types	66%	2.4
ICH GCP Firsts	63%	2.4
International Clinical Trials Day 2013: Clinical Trials Test	63%	2.4
GCP Challenge 52	43%	2.4
Oncology Trials	55%	2.4
Clinical Trial Design	52%	2.4
Top 20 Hardest Questions	43%	2.4
Abbreviations in CRFs	57%	2.4
ICH GCP Site Requirements	56%	2.4
ICH GCP - spelling it out	63%	2.4
ICH GCP Records and Reports	57%	2.4
Clinical Trial Statistics	47%	2.4
Biotechnology	55%	2.4
International Clinical Trials Day 2015	44%	2.4
ICH GCP - The Investigators Brochure	77%	2.5
Post marketing pharmacovigiliance	53%	2.4
ICH E6 GCP Addendum	52%	2.5
Abbreviations	55%	2.5
Pharmacovigilance for Clinical Trials	44%	2.5
ICH GCP Test	64%	2.5
ICH GCP Random questions	59%	2.5
Expanded Abbreviations	54%	2.5
The letter T	71%	2.5
Clinical Research Ethics	58%	2.5
New UK Legislation	48%	2.5
GCP 2008	40%	2.5
Biomarkers in Clinical Trials	65%	2.5
GCPGCP!	80%	2.5
ICH GCP - Descriptions	66%	2.5
Adverse Event Reporting	44%	2.5
Regulatory Authorities	65%	2.5
ICH GCP 25 Question Test	48%	2.5
ICH GCP Terminology	56%	2.5
ICH Defnitions	44%	2.5
Safety Reporting Abbreviations	55%	2.5
Bias in Clinical Trials	52%	2.5
Adverse Events	68%	2.6
ICH E3 Structure and Content of Clinical Study Reports	50%	2.6
The Letter B	50%	2.6
The letter B	72%	2.6
ICH GCP and the Protocol	51%	2.6
General ICH GCP	56%	2.6
ICH - Know Your Guidelines?	55%	2.6
Principles of ICH GCP	61%	2.6
ICH GCP - Filing Essential Documents	59%	2.6
Different Trial Designs	35%	2.6
Blinding in Clinical Trials	57%	2.6
ICH GCP - who is responsible?	61%	2.6
Declaration of Helsinki	59%	2.6
Clinical Research Odd Ones Out	48%	2.6
Clinical Research Systems	74%	2.6
Alternative Guidelines	51%	2.6
Specific Informed Consent Related Area	55%	2.6
EU Clinical Trials Regulation - New definitions	47%	2.6
The Letter E	65%	2.6
First Names in Pharmaceuticals	52%	2.6
ICH GCP Odd One Out	52%	2.6
Hardest GCP Related Questions	57%	2.6
Generic and Trade Names	50%	2.6
Pharma Industry facts and figures	48%	2.6
FESTIVE quiz	68%	2.6
Terms and names you may find in a protocol	40%	2.6
US Clinical Research	63%	2.6
Adverse Events - which category?	56%	2.6
ICH GCP General Questions III	59%	2.6
ICH GCP Definitions	70%	2.6
Ending and Suspending Trials	40%	2.6
Informed Consent (2)	48%	2.6
Seasonal Quiz	64%	2.6
Ultimate GCP II	61%	2.6
ICH GCP R2 Missing Words	57%	2.6
Clinical Trial Results	52%	2.6
ICH GCP - Who am I?	54%	2.6
ICH GCP - Who am I?	63%	2.6
ICH GCP and the Investigator	62%	2.6
Expected Adverse Events	52%	2.6
Clinical Research Abbreviation Connections	58%	2.6
ICH GCP Monitoring	43%	2.6
Statistics for Non-Statisticians	53%	2.6
Clinical Trial Assessments	77%	2.6
ICH GCP essential documents	59%	2.6
ICH GCP - What am I?	65%	2.6
Clinical Trial Databases	51%	2.6
Hardest 20 of 2011	34%	2.6
ICH GCP missing words 2	71%	2.6
Routes of Administration	73%	2.6
ICH GCP Study Closeout	66%	2.7
ICH GCP Committees	56%	2.7
Clinical Research 10	59%	2.7
Next in Sequence?	63%	2.7
Safety Reporting Abbreviations	56%	2.7
What Does GCP Say?	51%	2.7
Designing Clinical Trials	47%	2.7
GCP Definitions	62%	2.7
Abbreviations - P	68%	2.7
Odd One Out - Medications	49%	2.7
ICH GCP General Questions	60%	2.7
Essential Documents	64%	2.7
Reporting clinical trials	54%	2.7
ICH GCP - Trial Start Up	56%	2.7
Medical Devices 2	55%	2.7
Regulatory Agencies	52%	2.7
Investigational Medicinal Products	49%	2.7
FDA Guidance on the 1572 form	41%	2.7
GCP True or False	63%	2.7
Clinical Trials in Africa	45%	2.7
Industry Trivia	43%	2.7
History of Clinical Research	48%	2.7
Clinical Trials and Studies	46%	2.7
Document Control	66%	2.7
More AE case studies	47%	2.7
Clinical Trials Transparency	57%	2.7
The letter H	65%	2.7
Study Closeout	57%	2.7
Protocol Tests	45%	2.7
GCP Essential Documents 2	55%	2.7
Adverse events - case studies	47%	2.7
Key Milestones in GCP Guidelines	51%	2.7
Informed Consent	74%	2.7
Abbreviations 4	59%	2.7
ICH E11 - Clinical trials in children	61%	2.7
Project Management	57%	2.7
How much do you know about Clinical Research Part 1: History	58%	2.7
Guidelines, Legislation and Regulation	67%	2.7
EU Clinical Trials Regulation Timelines	54%	2.7
ICH GCP Monitoring - Missing words	63%	2.7
ICH GCP General Questions II	62%	2.7
ICH GCP General Questions IV	63%	2.7
ICH GCP Monitoring	65%	2.7
Ultimate Abbreviation Test	67%	2.7
ICH Pharmacovigilance	52%	2.7
ICH: If the question was...?	54%	2.7
A brief history of clinical trials	45%	2.7
ICH GCP 10	61%	2.7
Clinical Trial Statistics	50%	2.7
ICH GCP (R2) Monitoring	65%	2.7
The letter S	59%	2.8
ICH on Pharmacogenomics and Pharmacogenetics	51%	2.8
GCP Question Selection	65%	2.8
Statistics in Clinical Trials	66%	2.8
The Letter P	57%	2.8
In the Abbreviation	70%	2.8
ICH GCP Abbreviations	79%	2.7
E-GCP	70%	2.8
2012 GCP Test	57%	2.8
ICH GCP Investigational Products	69%	2.8
Concomitant Medications 2	62%	2.8
ICH GCP - Frequency of Terms	43%	2.8
Trial Design and Sample Size	44%	2.8
People in Medical Research	39%	2.8
Adaptive Trial Design	50%	2.8
ICH Missing Words	52%	2.8
What is missing from ICH?	64%	2.8
GCP Numbers	73%	2.8
Practical Hands On Sample Sizing	62%	2.8
Clinical Trial Project Management	48%	2.8
Declaration of Helsinki 2013	53%	2.8
Adverse Events - True or False	64%	2.8
Abbreviations	69%	2.8
Adverse Events	56%	2.8
GMP for IMP 2	51%	2.8
The Letter S	70%	2.8
ICHE6	70%	2.8
CRFs	71%	2.8
The Letter Q	66%	2.8
Clinical Trial Statistics	50%	2.8
Analysis Populations	56%	2.8
Risk in Clinical Trial Results	54%	2.8
Monitoring - Drug Types	74%	2.8
ICH GCP Missing Words	57%	2.8
GCP Test	69%	2.8
Statistics	58%	2.8
GCP - EU vs USA	49%	2.8
ICH Guidelines and Trial Design	51%	2.8
International Clinical Trials Day 2013: Ultimate GCP Test	67%	2.8
Adverse Events Surgical Case Studies	72%	2.8
Where in the world?	60%	2.8
Clinical Trials - Differences between EU and USA	53%	2.8
Ethics Committees in ICH GCP	54%	2.8
Relevant Numbers	61%	2.8
Legal and Financial Responsibility	64%	2.8
ICH GCP Definitions	60%	2.8
Random questions	55%	2.8
Informed Consent	63%	2.8
ICH E15	62%	2.8
Organisations	47%	2.8
Trial Results	54%	2.8
Best of 2017	59%	2.9
Pharmacovigilance in clinical trials	49%	2.8
Medical Devices	42%	2.9
Protocol Matters	57%	2.9
Clinical Trials in Children	53%	2.9
SPONSOR	72%	2.9
Placebo Controlled Trials	63%	2.9
AxMPs	62%	2.9
Odd One Out	42%	2.9
ICH GCP - What am I?	47%	2.9
Power and Sample Size	45%	2.9
ICH GCP - missing words	62%	2.9
Clinical Trials and GMP	51%	2.9
Statistical Tests	49%	2.9
GCP Inspections	69%	2.9
Clinical Trials Legislation, True or False	66%	2.9
SPRING quiz	60%	2.9
Risk Based Monitoring	67%	2.9
ICH Guidelines	58%	2.9
JUBILEE GCP	68%	2.9
Clinical Trials in the US	55%	2.9
GCP Revision	65%	2.9
The letter T	64%	2.9
21 CFR part 11 - Electronic Records and Electronic signatures	63%	2.9
ICH GCP Study Start-up	57%	2.9
The Letter A	66%	2.9
TRIAL	55%	2.9
Am I Right?	56%	2.9
How Much Do You Know About Clinical Research Part 3: Guidelines and Regulations	59%	2.9
Do I know my ICH?	61%	2.9
ICH GCP - which essential document?	69%	2.9
ICH GCP - Monitoring	71%	2.9
ICH GCP	66%	2.9
GCP Terminology - A	68%	2.9
21 CFR part 50	59%	2.9
Lab tests	62%	2.9
Updated ICH GCP and Related Guidelines	57%	2.9
Data Management in Clinical Trials	56%	2.9
Audits and Inspections	67%	2.9
Project Management	53%	2.9
True or False?	66%	2.9
GMP for IMP	54%	2.9
Clinical Laboratory Tests	79%	2.9
Top 25 Hardest Questions	36%	2.9
Clinical Trials in India	51%	2.9
Source Data	49%	2.9
Abbreviations	62%	2.9
FDA forms	63%	2.9
Adverse Events 10	73%	2.9
Informed Consent - case studies	57%	3
Clinicaltrials.gov II	67%	3
ICH GCP - A selection of questions	65%	3
ICH GCP: RESEARCH	51%	3
GCP Priority Scenario	42%	3
Who Am I?	65%	3
Hardest 20 Questions of 2015	41%	3
Monitoring	72%	3
Statistics in Trial Design True or False	59%	3
In the clinical laboratory	71%	3
ICH GCP Review	74%	3
EU Medical Devices Regulation	57%	3
ICH E2F - DSUR	54%	3
EMA policy on publication of clinical data	54%	3
ICH GCP - Monitor's Responsibilities	57%	3
ICH GCP Draft Addendum 2015	69%	3
The letter N	56%	3
International Abbreviations	89%	3
Clinical Trial Project Management	56%	3
Monitoring	73%	3
Global Companies	48%	3
GCP What is Missing?	55%	3
Famous Pharmaceuticals	65%	3
Declaration of Helsinki	56%	3
ICH - General Considerations for Clinical Trials	60%	3
Sample Sizing Clinical Trials	47%	3
2015 First Half: Hardest 10 Questions	44%	3
EU Clinical Trials Regulation (to be implemented 2016)	75%	3
Adverse Events	59%	3
ICH E Numbers	56%	3
The Investigator	64%	3
How much Do You Know About Clinical Research Part 5: Trial Results	55%	3
Hardest Questions of 2017	37%	3
Project Management	52%	3
ICH GCP - Who am I?	69%	3
Hardest 20 Questions of 2014	40%	3
Abbreviations 2	73%	3
Abbreviations in Clinical Research	73%	3
Data Management Terminology	46%	3
TRUE Questions	63%	3
ICH GCP Data Handling and Management	56%	3
Adverse Events Scenario	71%	3
In which country?	56%	3
ICH GCP: Can you do better?	65%	3
Ethics Committees	58%	3
ICH GCP - Does it say....?	66%	3
ICH - Adverse Events	54%	3
Industry Awareness	57%	3
The Letter C	71%	3
Electronic records and signatures - 21CFR part 11	65%	3.1
New Year	68%	3
Top 10 Most Challenging	45%	3.1
ICH GCP R2	60%	3.1
How Much Do You Know About Clinical Research Part 4: Conduct	61%	3.1
Project Management Terminology	59%	3.1
EASTER GCP	63%	3.1
Site Selection	50%	3.1
Clinical Trial Systems	60%	3.1
Geographical GCP	57%	3.1
Abbreviations 3	70%	3.1
Adverse Events 3	55%	3.1
GCP Combinations	58%	3.1
Know Your AEs?	71%	3.1
Adverse Events - ICH E2A	70%	3.1
Clinical Trial Writing	53%	3.1
ICH GCP - Investigator Responsibilities	62%	3.1
ICH GCP - Monitoring	71%	3.1
ICH GCP - The purpose of..	68%	3.1
EU Clinical Trials Regulation - GMP	57%	3.1
General Considerations for Clinical Trials	53%	3.1
EU Clinical Trials Legislation Quiz 2	50%	3.1
ICH E9 for Everybody	48%	3.1
Clinical Research Random Questions	66%	3.1
Trial Types and Design	54%	3.1
Pharmacokinetics	50%	3.1
Definitions and Abbreviations	54%	3.1
GCP Hardest Ten of 2010	51%	3.1
ICH GCP Definitions	66%	3.2
The Letter P	59%	3.2
Risk Based Monitoring	55%	3.2
Managing IMP	74%	3.2
History of ICH	48%	3.2
ICH GCP - Which document?	60%	3.2
Just Testing!	76%	3.2
Randomisation	50%	3.2
NEW YEAR	73%	3.2
ICH GCP True or False II	68%	3.2
EU Regulation on Clinical Trials	65%	3.2
The Letter A	65%	3.2
Clinical Trials	53%	3.2
What am I?	65%	3.2
Does ICH GCP Say?	69%	3.2
How Much Do You Know About Clinical Research Part 2: Methodology	56%	3.2
Serious Breaches	53%	3.2
The GCP Challenge of 2013	65%	3.2
Clinical Research - What is...?	59%	3.2
Research All Rounder	58%	3.2
ICH GCP: CLINICAL	65%	3.2
ICH GCP Trial Master Files	60%	3.2
Hardest 20 Questions of H1 2016	46%	3.2
Lets get CLINICAL	71%	3.2
ICH GCP Responsibilities	63%	3.2
GMP for IMP 3	48%	3.2
Understanding Data Management	63%	3.3
International Conference on Harmonisation	62%	3.3
16 Hardest Questions of 2016	37%	3.3
Understanding Data Management	59%	3.3
FDA Inspections	56%	3.3
ICH GCP Definitions	71%	3.3
The Letter M	67%	3.3
FDA Regulations	64%	3.3
Statistics in Clinical Trials 3	54%	3.3
Clinical Trials - Is this OK?	69%	3.3
Principles of ICH GCP	63%	3.3
ICH E8	68%	3.3
Ultimate GCP Challenge	56%	3.3
Drug Categories	79%	3.3
Top 10 Questions H1 2017	62%	3.3
Adverse Event cases	74%	3.3
Clinical Trials in Paediatrics - ICH E11	68%	3.3
EU GDPR	59%	3.3
Which document am I?	67%	3.3
ICH GCP Random questions	69%	3.3
Clinical Trial Statistics	57%	3.3
EASTER	74%	3.3
21CFR Random questions	53%	3.4
Clinical Trial Audit	64%	3.3
Ensuring Quality	75%	3.4
ICH E17 - MRCTs	62%	3.4
GCP - New EU requirements	49%	3.4
Statistics in Clinical Trials	53%	3.4
Clinical Trials and GDPR - Definitions	49%	3.4
Visual Clinical Research	80%	3.4
Abbreviations Odd One Out	41%	3.4
ICH GCP - The Protocol	60%	3.4
Managing Projects	66%	3.4
CRA Priority Scenario	64%	3.5
Adverse Events 2	74%	3.4
Electronic Informed Consent	74%	3.5
Clinical Trials in Canada	45%	3.5
21 CFR part 312	48%	3.5
16 Favourite Questions from 2016	59%	3.5
FDA Regulations 2	61%	3.6
Adverse Events 4	59%	3.6
Principles of ICH GCP	71%	3.7
Clinical Research and Chocolate	65%	3.7
Research All-Rounder	65%	3.7
Nobel Prize Winners	46%	3.8
Clinical Research All-Rounder	56%	3.9
TGN1412 incident	45%	3.9

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