Mots-clés
#clinical trials
#study conduct
#clinical research
#protocol
#rave
#protocol document
#clinical data management
#data base
#medidata
#medicine
#devices
#studystartup
#study closeout
#pharmaceutical industry
#post production changes
#ppc
# study conduct
#ecoa
#epro
#dynamics
#draft timelines
#cross functional team member
#stake holders
#range values
#structural functionality
##rave
#auto checks
3manual checks
#edit checks
#role testing
#uat
#edit check specification
ecrf
#vendor reconciliation
#medidate
#drug
#site
#doctor
#patient
#randomizarion
#double blinding
#open blinding
#bliniding
#lab
serious adverse event
#severe adverse effect
#adverse event
#safety data base
#irt
#database
#health
study
case study
clinical data management
#sae reconciliation
#reconciliation
#ich
#gcp
#study startup
#protocol amenment
#protocol deviation
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