Translation glossary: Clinical trial abbreviations

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BLLblinded line listing 
İngilizce
CIOMSCouncil for International Organizations of Medical Sciences 
İngilizce
CROcontract research organisation 
İngilizce
CTCAECommon Terminology Criteria for Adverse Events 
İngilizce
CTCAECommon Terminology Criteria for Adverse Events 
İngilizce
DSURdevelopment safety update report 
İngilizce
eCOAelectronic clinical outcome assessment 
İngilizce
eCRFelectronic case report form 
İngilizce
EOT visitend-of-trial visit 
İngilizce
EUCTREuropean Union Clinical Trials Register 
İngilizce
FAERSUS Food and Drug Administration Adverse Event Reporting System 
İngilizce
GCPGood Clinical Practice 
İngilizce
IBInvestigator\'s Brochure 
İngilizce
ICHInternational Council for Harmonisation of Technical Requirements of Pharmaceuticals for Human Use 
İngilizce
ICH GCPInternational Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) Guideline for Good Clinical Practice (GCP). 
İngilizce
ICRindependent central review 
İngilizce
IMPinvestigational medicinal product 
İngilizce
IRASIntegrated Research Application System 
İngilizce
IRBInstitutional Review Board 
İngilizce
ISFInvestigator Site File 
İngilizce
IWRSinteractive web response system 
İngilizce
PGAPhysician Global Assessment [sometimes \'Patient Global Assessment\'] 
İngilizce
PIPrincipal Investigator [responsible for each research site; distinguish from Chief Investigator] 
İngilizce
PIS/ICFParticipant Information Sheet and Informed Consent Form 
İngilizce
pMCSpartial Mayo Clinic Score 
İngilizce
SCStudy Coordinator 
İngilizce
SFscreen failure [patient who did not pass screening] 
İngilizce
SIVsite initiation visit 
İngilizce
SOPsStandard Operating Procedures 
İngilizce
Sub-ISub-Investigator 
İngilizce
UVunscheduled visit 
İngilizce
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