PharmaSchool: GCP & Clinical Research Tests and Challenges

Quiz Title ( All )	Average Score	User Rating	Rating
Clinical Research Random Questions	67%	3.1
GCP by Numbers	45%	2.3
EU Medical Devices Regulation	56%	3
Risk Based Monitoring	55%	3.1
Trial Types and Design	54%	3.1
Randomisation	50%	3.1
Industry Awareness	57%	3
True or False?	66%	2.8
Clinical Trials and GDPR - Definitions	49%	3.1
EASTER	74%	3.1
What am I?	64%	3.1
Data Management Terminology	46%	3
Adverse Events	58%	3
Statistics in Trial Design True or False	59%	2.8
ICH E Numbers	56%	2.9
ICH GCP Responsibilities	63%	3.2
Project Management	52%	3
ICH E17 - MRCTs	62%	3.3
ICH GCP (R2) Monitoring	65%	2.7
ICH GCP R2 Missing Words	57%	2.6
NEW YEAR	73%	3.2
Hardest Questions of 2017	37%	3
Best of 2017	59%	2.9
ICH GCP - Who am I?	63%	2.6
Statistics for Non-Statisticians	52%	2.6
Monitoring	71%	2.9
EU GDPR	59%	3.1
21CFR Random questions	53%	3.3
Research All Rounder	58%	3.2
Source Data	49%	3
The letter N	56%	2.9
Understanding Data Management	59%	3.3
The Investigator	64%	2.9
AxMPs	62%	2.8
Project Management Terminology	59%	3.1
ICHE6	70%	2.8
Top 10 Questions H1 2017	62%	3.3
Informed Consent	63%	2.8
The letter S	59%	2.8
Clinical Trial Project Management	47%	2.8
TRUE Questions	63%	3
ICH GCP Definitions	71%	3.3
Research All-Rounder	65%	3.8
TRIAL	55%	2.9
Clinical Trial Results	52%	2.6
Lets get CLINICAL	70%	3.3
History of ICH	48%	3.2
Managing Projects	66%	3.4
Which document am I?	67%	3.3
Ensuring Quality	75%	3.3
Trial Results	54%	2.8
ICH GCP Random questions	69%	3.3
Understanding Data Management	63%	3.3
Where in the world?	61%	2.8
Am I Right?	55%	2.9
The Letter B	49%	2.5
ICH E8	68%	3.3
Project Management	56%	2.7
The letter H	65%	2.7
Just Testing!	76%	3.2
Electronic Informed Consent	73%	3.5
Keeping Research in Order	44%	2.4
Adverse Event cases	74%	3.3
Updated ICH GCP and Related Guidelines	57%	2.9
ICH GCP R2	60%	3.1
16 Hardest Questions of 2016	37%	3.2
16 Favourite Questions from 2016	59%	3.5
Abbreviations	55%	2.5
ICH GCP - Investigator Responsibilities	62%	3.1
Clinical Trial Systems	59%	3.1
Organisations	47%	2.8
Clinical Trials	52%	3.2
ICH GCP Monitoring - Missing words	63%	2.8
GCP Inspections	69%	2.9
Numbers	47%	2.3
The Letter P	59%	3.2
General Considerations for Clinical Trials	53%	3.1
Project Management	53%	2.9
Clinical Trials - Is this OK?	69%	3.3
Hardest 20 Questions of H1 2016	47%	3.2
Document Control	66%	2.7
E Numbers	61%	2.1
ICH GCP - Monitoring	71%	3.1
Clinicaltrials.gov II	67%	3
Who Am I?	65%	3
Analyses	49%	2.3
Principles of ICH GCP	63%	3.3
Audits and Inspections	67%	2.9
ICH GCP - A selection of questions	65%	3
EU Clinical Trials Regulation - GMP	57%	3.1
Statistical Tests	49%	2.9
Lab tests	61%	2.9
The Letter Q	66%	2.8
Adverse Events - ICH E2A	70%	3.1
Legal and Financial Responsibility	64%	2.9
Data Management in Clinical Trials	56%	2.9
Expanded Abbreviations	53%	2.5
EU Clinical Trials Regulation - New definitions	47%	2.6
The Letter E	65%	2.6
Abbreviations	62%	2.9
Clinical Trial Databases	51%	2.6
Alternative Guidelines	51%	2.6
GCP Numbers	73%	2.8
Medical Devices 2	55%	2.7
Next in Sequence?	63%	2.7
21 CFR part 50	59%	2.9
Clinical Trial Statistics	47%	2.4
New Year	68%	3
Hardest 20 Questions of 2015	41%	3
Early Phase Trials	54%	2.4
ICH E15	62%	2.8
EU Regulation on Clinical Trials	65%	3.2
Safety Reporting Abbreviations	56%	2.7
ICH GCP Random questions	59%	2.5
Analysis Populations	56%	2.8
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
Biotechnology	55%	2.4
ICH E2F - DSUR	54%	3
Clinical Trial Statistics	49%	2.7
The letter B	72%	2.6
Clinical Trial Project Management	56%	3
2015 First Half: Hardest 10 Questions	44%	3
Clinical Trials Legislation, True or False	66%	2.9
Specific Informed Consent Related Area	55%	2.6
ICH E11 - Clinical trials in children	61%	2.7
In the Abbreviation	70%	2.8
FDA forms	63%	2.9
Guideline Updates and Additions	51%	2.4
ICH GCP Words and Terms	48%	2.3
Protocol Tests	45%	2.7
International Clinical Trials Day 2015	44%	2.4
Clinical Research 10	59%	2.7
Adverse Events 10	73%	2.9
ICH GCP 10	61%	2.7
Adverse Events - True or False	64%	2.8
Electronic records and signatures - 21CFR part 11	65%	3.1
Guidelines, Legislation and Regulation	66%	2.7
The Letter P	57%	2.8
EU Clinical Trials Legislation Quiz 2	50%	3.1
Legislation or Guidance?	71%	2.4
ClinicalTrials.gov	39%	2.1
Clinical Research Systems	74%	2.6
Clinical Research Odd Ones Out	47%	2.6
Adverse Events	68%	2.6
Clinical Trial Statistics	49%	2.8
EMA policy on publication of clinical data	54%	3
ICH GCP - missing words	62%	2.9
ICH GCP and the Protocol	51%	2.6
CRFs	71%	2.8
History of Clinical Research	48%	2.7
Hardest 20 Questions of 2014	40%	3
SPONSOR	72%	2.9
Regulatory Agencies	52%	2.7
Clinical Trial Writing	53%	3.1
The Letter M	67%	3.3
EU Clinical Trials Regulation Timelines	54%	2.7
Clinical Trials and Studies	46%	2.7
ICH GCP Abbreviations	79%	2.7
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
Top 10 Most Challenging	45%	3.1
GCP Revision	65%	2.9
ICH GCP - Who am I?	55%	2.6
Bias in Clinical Trials	52%	2.5
The letter T	64%	2.9
Clinical Trial Statistics	57%	3.3
Informed Consent - case studies	57%	3
A brief history of clinical trials	45%	2.7
Clinical Trials - Differences between EU and USA	53%	2.9
Safety Reporting Abbreviations	55%	2.5
ICH GCP - What am I?	65%	2.6
EU Clinical Trials Regulation (to be implemented 2016)	75%	3
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
SPRING quiz	60%	2.9
ICH GCP Odd One Out	52%	2.6
General ICH GCP	58%	2.3
Managing IMP	74%	3.2
Practical Hands On Sample Sizing	62%	2.8
ICH E9 for Everybody	48%	3.1
How much Do You Know About Clinical Research Part 5: Trial Results	55%	3
How Much Do You Know About Clinical Research Part 4: Conduct	61%	3.1
How Much Do You Know About Clinical Research Part 3: Guidelines and Regulations	59%	2.9
How Much Do You Know About Clinical Research Part 2: Methodology	55%	3.2
How much do you know about Clinical Research Part 1: History	58%	2.7
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
Clinical Trial Audit	64%	3.3
ICH GCP True or False II	68%	3.2
Visual Clinical Research	80%	3.4
Geographical GCP	57%	3.1
Random questions	54%	2.8
In the clinical laboratory	71%	3
Know Your AEs?	71%	3.1
ICH GCP - Who am I?	69%	3
ICH GCP Review	74%	3
International Abbreviations	88%	3
ICH GCP Firsts	63%	2.4
ICH GCP Study Closeout	66%	2.7
Reporting clinical trials	54%	2.7
Compassionate Use	47%	2.3
ICH GCP Terminology	56%	2.5
Do I know my ICH?	61%	2.9
ICH GCP Investigational Products	69%	2.8
ICH GCP Investigational Product	48%	2.3
The letter T	71%	2.5
FDA Inspections	56%	3.3
Abbreviations - P	68%	2.7
Informed Consent in ICH GCP	60%	2.4
Declaration of Helsinki	59%	2.6
Pharmacovigilance for Clinical Trials	44%	2.5
ICH GCP - Principles	66%	2.3
Hardest 20 of 2011	34%	2.6
General ICH GCP	56%	2.6
GCPGCP!	80%	2.6
Ordering GCP	59%	2.1
ICH GCP Data Handling and Management	56%	3
Advanced Therapies	48%	2.4
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
EASTER GCP	64%	3.1
ICH GCP - Monitoring	65%	2.3
In which country?	55%	3
ICH GCP Definitions	70%	2.6
Monitoring - Drug Types	74%	2.8
GCP - EU vs USA	49%	2.8
E-GCP	70%	2.8
What is missing from ICH?	64%	2.8
Key Milestones in GCP Guidelines	50%	2.7
Study Closeout	57%	2.7
Understanding Endpoints	52%	2.1
Sample Sizing for Clinical Researchers	58%	1.8
Informed Consent Documents	44%	2.2
Statistics in Clinical Trials	66%	2.8
Do you know your ICH GCP?	67%	2.4
ICH GCP - The purpose of..	68%	3.1
International Clinical Trials Day 2013: Clinical Trials Test	63%	2.2
International Clinical Trials Day 2013: Ultimate GCP Test	67%	2.8
ICH GCP Study Start-up	57%	2.9
The Letter C	71%	3
GCP, Guides, Books and Colours	49%	2
Adverse Events Surgical Case Studies	72%	2.8
Keeping ICH in Order	52%	2
Principles of ICH GCP	71%	3.7
Pharma Industry facts and figures	48%	2.6
ICH: If the question was...?	54%	2.7
Risk Based Monitoring	67%	2.9
Post marketing pharmacovigiliance	52%	2.4
Proposed new EU legislation on Clinical Trials	47%	1.8
ABC of Clinical Trials	58%	2.1
ICH on Pharmacogenomics and Pharmacogenetics	52%	2.8
Product Types and Uses	66%	2.4
2012 GCP Test	57%	2.8
ICH GCP - random questions	59%	2.2
First Names in Pharmaceuticals	52%	2.6
ICH GCP - The Investigators Brochure	77%	2.5
GCP Question Selection	65%	2.8
ICH Guidelines and Trial Design	51%	2.8
Risk in Clinical Trial Results	54%	2.8
ICH GCP Test	64%	2.5
Clinical Trials Transparency	57%	2.7
ICH GCP Informed Consent	90%	2.3
JUBILEE GCP	68%	2.9
Who is responsible for?	53%	2
The Letter A	66%	2.9
Pharmacokinetics	50%	3.1
Clinical Trials in Africa	45%	2.7
GCP True or False	63%	2.7
ICH GCP Test	48%	2.3
Recruitment and Consent	59%	2
Clinical Trial Assessments	77%	2.6
1, 2, 3, 4, 5 ....... ICH	54%	2.2
Drug Life Cycle Terms	53%	2.2
Foreign Clinical Trials	70%	1.3
Welcome to 2013	48%	2.2
Hardest 20 of 2012	48%	2.1
ICH GCP - which essential document?	68%	2.9
21 CFR part 312	48%	3.5
ICH E2A - Safety First	47%	2.2
Clinical Research - What is...?	59%	3.2
Approvals and Global Sales	46%	1.2
GCP in Asia	40%	2.2
Ending and Suspending Trials	41%	2.6
GCP Revision 2011 Half 1	37%	1.8
ICH GCP Monitoring	65%	2.7
ICH GCP Records and Reports	57%	2.4
ICH Guideline E2F DSURs	48%	1.6
ICH GCP - spelling it out	63%	2.4
Choice of control for clinical trials - ICH E10	50%	2.4
Different Trial Designs	35%	2.6
Adverse Events Scenario	71%	3
April GCP Updates	49%	2
Clinical Trials in Children	53%	2.9
ICH GCP General Questions III	59%	2.6
ICH - Know Your Guidelines?	55%	2.6
ICH Pharmacovigilance	52%	2.7
History of the FDA	45%	2.4
ICH GCP - Filing Essential Documents	59%	2.6
Getting Products to Market	46%	1.4
GCP Terminology - A	68%	2.9
ICH - General Considerations for Clinical Trials	60%	3
Clinical Trial Measurement Scales	46%	2.2
ICH GCP - Training	60%	2
More AE case studies	47%	2.7
Informed Consent	52%	1.8
Drug Categories	79%	3.3
Guidelines for?	58%	2.2
ICH GCP - Does it say....?	67%	3
Serious Breaches	52%	3.2
The Letter O	72%	1.4
GCP Hardest Ten of 2010	51%	3.1
PharmaSchool Favourites	47%	2.3
Regulatory - What is it? II	44%	2
Regulatory What Is It?	37%	1.8
GCP Priority Scenario	43%	3
CRA Priority Scenario	64%	3.5
Clinical Research Definitions	63%	1.8
ICH GCP - Informed Consent	56%	2.4
IMPs in ICH GCP	56%	1.7
US Clinical Research	63%	2.6
Statistics in Protocols	47%	2.3
Designs of Clinical Trials	47%	2.3
Routes of Administration	73%	2.6
Famous Pharmaceuticals	65%	3
ICH GCP definitions	56%	2.3
GCP Combinations	58%	3.1
Clinical Trials in Canada	45%	3.5
ICH GCP - Investigational Products	55%	2.4
ICH GCP General Questions II	62%	2.8
Clinical Study Reports	45%	1.3
Clinical Research Ethics	57%	2.5
Odd one out	42%	1.8
Pharmacovigilance in clinical trials	49%	2.8
Regulatory Agencies	46%	1.9
ICH GCP - Investigator responsibilities	56%	2.4
International Clinical Trials	49%	1
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
Site Selection	50%	3.1
ICH GCP Trial Master Files	60%	3.2
GCP Lists	52%	0.8
Interpreting Trial Results	41%	1.6
ICH GCP and the CRO	59%	1.8
ICH GCP Insurance and Indemnity	54%	1.8
Protocol Matters	56%	2.9
ICH GCP - what do these have in common?	66%	2.4
ICH GCP Test	57%	2
Seasonal Competition Quiz	42%	2.4
ICH Trial Results Related Definitions	54%	1.2
Informed Consent - Subject Information	59%	1.8
Clinical Trial Permissions	41%	1.9
Informed Consent - missing words	64%	2.4
Sum More GCP	44%	1.1
GCP	56%	2.2
ICH GCP - Informed Consent	63%	2.3
ICH GCP - Investigator Qualifications and Agreements	54%	2.1
FDA - new regulation governing foreign clinical trials	43%	2.1
Monitoring	73%	3
Ethics Committees (2)	51%	1.9
Ultimate Abbreviation Test	66%	2.7
What's the difference?	57%	1.4
25 Question GCP and CR Test	57%	2.2
ICH E10 Choice Of Control Group	39%	2.3
Adverse Events - which category?	56%	2.6
Clinical Trial Percentages	52%	1.8
ICH E16	54%	2
GCP Update 2010	52%	1.7
Industry Update	40%	0.8
Clinical Trial Phases	49%	2.1
ICH GCP - Monitoring	71%	2.9
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
Clinical Research Abbreviation Connections	58%	2.6
Clinical Research - Things I Should Know	62%	2.1
Clinical Trial Design 3	49%	2.2
The Letter C	68%	1.1
Designing Clinical Trials	47%	2.7
Geographical GCP	42%	1.5
ICH - Adverse Events	54%	3
Terms and names you may find in a protocol	40%	2.6
International GCP Guidelines	51%	2.2
ICH GCP IRB and IEC	51%	2.2
Sample Sizing Clinical Trials	47%	3
The International Conference on Harmonisation	45%	1.7
Definitions and Abbreviations	54%	3.1
ICH GCP Multicentre Trials	54%	2.4
Clinical Research Forms	54%	1.7
Abbreviations in Clinical Research	73%	3
GCP Compliance	57%	2.4
Seasonal Quiz	64%	2.6
2008 version of Declaration of Helsinki	59%	2.3
Clinical Research All-Rounder II	46%	1.7
ICH and GCP Numbers	62%	2
The Letter S	70%	2.8
ICH GCP - Frequency of Terms	43%	2.8
ICH GCP - What is the Question?	51%	2
International GCP Update	40%	2
ICH GCP - The Protocol	60%	3.4
Expected Adverse Events	52%	2.6
The letter G	60%	1.2
Orphan Drugs	38%	1.8
GCP Challenge 52	43%	2.4
Clinical Systems and Software	39%	1
More Abbreviations	68%	2.4
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
Odd One Out - Medications	49%	2.7
ICH GCP Site Requirements	56%	2.4
What's in a name?	42%	1.9
Medications and Medication Types	66%	2.4
Know your GCP	46%	1.8
ICH GCP - Monitor's Responsibilities	57%	3
What Does GCP Say?	51%	2.7
Famous Pharmaceutical Companies	54%	1.6
Ethics Committees in ICH GCP	54%	2.8
ICH GCP Audits	49%	2.3
Global Companies	48%	3
Christmas GCP	54%	1
Concomitant Medications 2	62%	2.8
ICH GCP - What is the difference?	62%	2.4
Adverse events - case studies	47%	2.7
Who am I?	34%	1.8
Subject Recruitment	65%	1.8
Clinical Trials: What's the difference?	36%	1.7
ICH GCP Informed Consent Section	63%	2.3
GCP 2008	40%	2.5
Sections of ICH GCP	47%	1.4
Concomitant Medication	72%	2.4
Protocol Design	41%	2.2
Ultimate GCP II	61%	2.6
IRB vs IEC	49%	1.5
GCP Inspections	46%	1.8
Declaration of Helsinki	56%	3
GCP - Who am I?	67%	1.8
Clinical Trial Measurements	60%	2.3
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
Pharmaceuticals in Modern Culture	44%	2.2
IMP labelling	47%	2.2
Power and Sample Size	45%	2.9
Informed Consent - Missing Words	61%	1.6
GCP.......What Next?	39%	1.7
Adaptive Trial Design	50%	2.8
Biomarkers in Clinical Trials	65%	2.5
Adverse Event Reporting	44%	2.6
Sum GCP!	51%	2.1
Abbreviations Odd One Out	41%	3.4
Abbreviations in CRFs	57%	2.4
ICH GCP Audits	51%	2.5
General ICH GCP Questions	61%	2.2
GMP for IMP 4	42%	2.2
What is?	51%	1.7
Medical Abbreviations	74%	2.2
New UK Legislation	48%	2.5
ICH GCP Section 6	46%	2.1
Laboratory Tests	70%	1.6
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
FESTIVE quiz	68%	2.6
Hardest GCP Related Questions	57%	2.6
GCP Essential Documents 2	55%	2.7
Adverse Events 4	59%	3.6
GCP - New EU requirements	49%	3.4
ICH GCP	66%	2.9
Health Economics	37%	2.4
Health Economics in the UK	34%	2
Trial Design and Sample Size	44%	2.8
Blinding in Clinical Trials	57%	2.6
Statistics in Clinical Trials 3	54%	3.3
Adverse Events 3	55%	3.1
People in Medical Research	39%	2.8
Clinical Pharmacology	62%	1.7
Generic and Trade Names	50%	2.6
Where would you find...............?	47%	1.5
ICH GCP Missing Words	57%	2.8
Clinical Laboratory Tests 2	68%	1.9
The Letter P	70%	1.6
FDA Regulations	64%	3.3
Name the year	51%	2.2
Clinical Research and Chocolate	65%	3.7
ICH GCP: RESEARCH	51%	3
ICH GCP: CLINICAL	65%	3.2
Top 25 Hardest Questions	36%	2.9
Trial Design 2	54%	2.3
TGN1412 incident	45%	3.9
Informed Consent (2)	48%	2.6
ICH GCP missing words 2	71%	2.6
Nobel Prize Winners	46%	3.8
The Letter T	60%	2.3
ICH Missing Words (2)	58%	2.4
The Letter A	65%	3.2
Statistics in Clinical Trials	53%	3.4
Top 20 Hardest Questions	43%	2.4
Clinical Laboratory Tests	79%	2.9
Adverse Events 2	74%	3.4
Pharma Industry	42%	2.4
Odd One Out	42%	2.9
ICH Missing Words	52%	2.8
Ultimate GCP Challenge	56%	3.3
Randomisation	47%	2.3
Clinical Research All-Rounder	56%	3.9
Abbreviations 4	59%	2.7
GMP for IMP 3	48%	3.2
Ethics Committees	58%	3
Informed Consent	74%	2.7
Medical Devices	42%	2.9
GMP for IMP 2	51%	2.8
Adverse Events	56%	2.8
Abbreviations 3	70%	3.1
Clinical Trial Design	52%	2.4
Regulatory Authorities	65%	2.5
ICH Guidelines	57%	2.9
Oncology Trials	55%	2.5
Essential Documents	64%	2.7
Industry Trivia	43%	2.7
GMP for IMP	54%	3
Abbreviations 2	73%	3
EU Directives	48%	2.4
Relevant Numbers	61%	2.8
Abbreviations	69%	2.8
Statistics	58%	2.8
GCP Test	69%	2.8