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pharmaschool: gcp & clinical research tests and challenges home page | in-house courses | online courses | tests & challenges | resources | cvc check about pharmaschool | contact 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 number of challenges & tests taken to date: 825,919 gcp & guidelines | trial design | adverse events | monitoring | statistics | abbreviations | general | show all quiz title ( all ) average score user rating rating clinical research random questions 62% 3.3 gcp by numbers 42% 2.3 eu medical devices regulation 59% 3.6 risk based monitoring 58% 3.6 trial types and design 59% 3.8 randomisation 59% 3.7 industry awareness 58% 3.2 true or false? 68% 3.2 clinical trials and gdpr - definitions 55% 3.9 easter 75% 3.5 what am i? 70% 3.5 data management terminology 49% 3.2 adverse events 65% 3.2 statistics in trial design true or false 66% 3.4 ich e numbers 57% 3 ich gcp responsibilities 66% 3.6 project management 57% 3.3 ich e17 - mrcts 63% 3.8 ich gcp (r2) monitoring 68% 2.9 ich gcp r2 missing words 56% 3 new year 75% 3.6 hardest questions of 2017 39% 3.2 best of 2017 60% 3 ich gcp - who am i? 65% 3.1 statistics for non-statisticians 55% 2.7 monitoring 75% 3.2 eu gdpr 60% 3.5 21cfr random questions 55% 3.4 research all rounder 61% 3.3 source data 52% 3 the letter n 54% 3.3 understanding data management 62% 3.3 the investigator 65% 3.2 axmps 62% 2.9 project management terminology 61% 3.2 iche6 71% 2.9 top 10 questions h1 2017 62% 3.4 informed consent 66% 3.1 the letter s 60% 3 clinical trial project management 50% 2.7 true questions 65% 3.2 ich gcp definitions 73% 3.4 research all-rounder 67% 3.9 trial 57% 2.9 clinical trial results 54% 2.7 lets get clinical 72% 3.4 history of ich 48% 3.3 managing projects 69% 3.5 which document am i? 69% 3.5 ensuring quality 77% 3.5 trial results 55% 3.1 ich gcp random questions 71% 3.5 understanding data management 65% 3.4 where in the world? 61% 2.8 am i right? 56% 3 the letter b 50% 2.6 ich e8 69% 3.6 project management 58% 2.8 the letter h 67% 2.8 just testing! 77% 3.3 electronic informed consent 76% 3.5 keeping research in order 47% 2.4 adverse event cases 76% 3.4 updated ich gcp and related guidelines 57% 3.1 ich gcp r2 61% 3.1 16 hardest questions of 2016 36% 3.4 16 favourite questions from 2016 61% 3.6 abbreviations 56% 2.4 ich gcp - investigator responsibilities 65% 3.3 clinical trial systems 62% 3.2 organisations 48% 3.1 clinical trials 54% 3.3 ich gcp monitoring - missing words 62% 2.8 gcp inspections 71% 3.1 numbers 48% 2.4 the letter p 61% 3.3 general considerations for clinical trials 54% 3.2 project management 53% 3.1 clinical trials - is this ok? 71% 3.4 hardest 20 questions of h1 2016 47% 3.3 document control 68% 2.7 e numbers 62% 2.2 ich gcp - monitoring 71% 3.2 clinicaltrials.gov ii 69% 3 who am i? 66% 3 analyses 50% 2.5 principles of ich gcp 64% 3.4 audits and inspections 68% 2.9 ich gcp - a selection of questions 66% 3 eu clinical trials regulation - gmp 58% 3.2 statistical tests 49% 3 lab tests 62% 3 the letter q 66% 2.8 adverse events - ich e2a 71% 3.2 legal and financial responsibility 64% 2.9 data management in clinical trials 59% 2.9 expanded abbreviations 54% 2.6 eu clinical trials regulation - new definitions 47% 2.7 the letter e 64% 2.7 abbreviations 63% 3 clinical trial databases 52% 2.7 alternative guidelines 52% 2.7 gcp numbers 73% 2.9 medical devices 2 57% 2.8 next in sequence? 63% 2.9 21 cfr part 50 59% 3.1 clinical trial statistics 48% 2.5 new year 68% 3.1 hardest 20 questions of 2015 43% 3 early phase trials 56% 2.4 ich e15 63% 3 eu regulation on clinical trials 67% 3.2 safety reporting abbreviations 58% 2.7 ich gcp random questions 59% 2.5 analysis populations 59% 2.9 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% 3 biotechnology 56% 2.6 ich e2f - dsur 55% 3.1 clinical trial statistics 52% 2.8 the letter b 72% 2.7 clinical trial project management 57% 3.1 2015 first half: hardest 10 questions 45% 3.1 clinical trials legislation, true or false 67% 3 specific informed consent related area 55% 2.6 ich e11 - clinical trials in children 61% 2.8 in the abbreviation 71% 2.8 fda forms 64% 3 guideline updates and additions 52% 2.5 ich gcp words and terms 48% 2.3 protocol tests 46% 2.7 international clinical trials day 2015 44% 2.5 clinical research 10 60% 2.7 adverse events 10 74% 3 ich gcp 10 63% 2.7 adverse events - true or false 65% 2.8 electronic records and signatures - 21cfr part 11 66% 3.1 guidelines, legislation and regulation 69% 2.8 the letter p 58% 2.8 eu clinical trials legislation quiz 2 50% 3.3 legislation or guidance? 72% 2.4 clinicaltrials.gov 40% 2.2 clinical research systems 76% 2.7 clinical research odd ones out 48% 2.6 adverse events 69% 2.6 clinical trial statistics 51% 3 ema policy on publication of clinical data 56% 3 ich gcp - missing words 63% 2.9 ich gcp and the protocol 52% 2.6 crfs 72% 2.8 history of clinical research 50% 2.7 hardest 20 questions of 2014 41% 3.1 sponsor 74% 2.9 regulatory agencies 54% 2.7 clinical trial writing 53% 3.1 the letter m 68% 3.3 eu clinical trials regulation timelines 55% 2.7 clinical trials and studies 47% 2.7 ich gcp abbreviations 80% 2.8 placebo controlled trials 64% 2.9 clinical trials in the us 57% 3 clinical trials and gmp 54% 2.9 ich e6 gcp addendum 53% 2.5 clinical trials in paediatrics - ich e11 69% 3.4 ich defnitions 45% 2.6 top 10 most challenging 45% 3.1 gcp revision 66% 2.9 ich gcp - who am i? 55% 2.6 bias in clinical trials 54% 2.5 the letter t 65% 3 clinical trial statistics 59% 3.4 informed consent - case studies 57% 3 a brief history of clinical trials 45% 2.8 clinical trials - differences between eu and usa 53% 2.7 safety reporting abbreviations 56% 2.6 ich gcp - what am i? 66% 2.7 eu clinical trials regulation (to be implemented 2016) 76% 3 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 spring quiz 61% 2.9 ich gcp odd one out 52% 2.6 general ich gcp 59% 2.3 managing imp 75% 3.2 practical hands on sample sizing 66% 2.8 ich e9 for everybody 48% 3.1 how much do you know about clinical research part 5: trial results 57% 3 how much do you know about clinical research part 4: conduct 62% 3.1 how much do you know about clinical research part 3: guidelines and regulations 60% 2.9 how much do you know about clinical research part 2: methodology 56% 3.2 how much do you know about clinical research part 1: history 59% 2.7 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 clinical trial audit 65% 3.4 ich gcp true or false ii 69% 3.2 visual clinical research 81% 3.4 geographical gcp 58% 3.1 random questions 55% 2.9 in the clinical laboratory 71% 3.1 know your aes? 71% 3.1 ich gcp - who am i? 70% 3 ich gcp review 75% 3 international abbreviations 90% 3 ich gcp firsts 64% 2.5 ich gcp study closeout 66% 2.7 reporting clinical trials 55% 2.8 compassionate use 47% 2.6 ich gcp terminology 56% 2.5 do i know my ich? 62% 3 ich gcp investigational products 70% 2.9 ich gcp investigational product 49% 2.4 the letter t 72% 2.6 fda inspections 57% 3.3 abbreviations - p 68% 3 informed consent in ich gcp 60% 2.4 declaration of helsinki 60% 2.7 pharmacovigilance for clinical trials 45% 2.5 ich gcp - principles 67% 2.4 hardest 20 of 2011 34% 2.8 general ich gcp 56% 2.6 gcpgcp! 80% 2.7 ordering gcp 59% 2.3 ich gcp data hand

URL analysis for pharmaxm.com

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Whois Information

Whois is a protocol that is access to registering information. You can reach when the website was registered, when it will be expire, what is contact details of the site with the following informations. In a nutshell, it includes these informations;

Whois Server Version 2.0

Domain names in the .com and .net domains can now be registered
with many different competing registrars. Go to http://www.internic.net
for detailed information.

Domain Name: PHARMAXM.COM
Registrar: TUCOWS DOMAINS INC.
Sponsoring Registrar IANA ID: 69
Whois Server: whois.tucows.com
Referral URL: http://www.tucowsdomains.com
Name Server: NS1.LIVEDNS.CO.UK
Name Server: NS2.LIVEDNS.CO.UK
Name Server: NS3.LIVEDNS.CO.UK
Status: clientTransferProhibited http://www.icann.org/epp#clientTransferProhibited
Status: clientUpdateProhibited http://www.icann.org/epp#clientUpdateProhibited
Updated Date: 09-jul-2015
Creation Date: 08-aug-2007
Expiration Date: 08-aug-2017

>>> Last update of whois database: Wed, 15 Jul 2015 14:01:54 GMT <<<

NOTICE: The expiration date displayed in this record is the date the
registrar's sponsorship of the domain name registration in the registry is
currently set to expire. This date does not necessarily reflect the expiration
date of the domain name registrant's agreement with the sponsoring
registrar. Users may consult the sponsoring registrar's Whois database to
view the registrar's reported date of expiration for this registration.

TERMS OF USE: You are not authorized to access or query our Whois
database through the use of electronic processes that are high-volume and
automated except as reasonably necessary to register domain names or
modify existing registrations; the Data in VeriSign Global Registry
Services' ("VeriSign") Whois database is provided by VeriSign for
information purposes only, and to assist persons in obtaining information
about or related to a domain name registration record. VeriSign does not
guarantee its accuracy. By submitting a Whois query, you agree to abide
by the following terms of use: You agree that you may use this Data only
for lawful purposes and that under no circumstances will you use this Data
to: (1) allow, enable, or otherwise support the transmission of mass
unsolicited, commercial advertising or solicitations via e-mail, telephone,
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The Registry database contains ONLY .COM, .NET, .EDU domains and
Registrars.

For more information on Whois status codes, please visit
https://www.icann.org/resources/pages/epp-status-codes-2014-06-16-en.

  REGISTRAR TUCOWS DOMAINS INC.

  REFERRER http://www.tucowsdomains.com

SERVERS

  SERVER com.whois-servers.net

  ARGS domain =pharmaxm.com

  PORT 43

  SERVER whois.tucows.com

  ARGS pharmaxm.com

  PORT 43

  TYPE domain

DOMAIN

  NAME pharmaxm.com

NSERVER

  NS1.LIVEDNS.CO.UK 213.171.192.250

  NS2.LIVEDNS.CO.UK 213.171.193.250

  NS3.LIVEDNS.CO.UK 213.171.192.254

STATUS
clientTransferProhibited http://www.icann.org/epp#clientTransferProhibited
clientUpdateProhibited http://www.icann.org/epp#clientUpdateProhibited

  CHANGED 2015-07-09

  CREATED 2007-08-08

  EXPIRES 2017-08-08

  REGISTERED yes

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