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问题		答案
AACI 开始学习		association of american cancer issues
abm 开始学习		agencja badań medycznych
adr 开始学习		adverse drug reaction
ae 开始学习		adverse event
aha 开始学习		american heart association
alcoa 开始学习		attributable legible contemporaneous orginal accurate complete
amc 开始学习		academic medical center
aotmit 开始学习		agencja oceny technologii medycznych i taryfikacji
api 开始学习		active pharmaceutical ingredient
aro 开始学习		academic research organization
asap 开始学习		as soon as possible
atc 开始学习		anatomic therapeutic chemicsl coding dictionary
auc 开始学习		Area under the curve
bid 开始学习		twice daily
bsa 开始学习		body surface area
ca 开始学习		competent authority
ca 开始学习		comfidentiallity agreement
capa 开始学习		corrective and preventive action
ccea 开始学习		complete consistent endurong available
ccm 开始学习		concomitant medication
ccr 开始学习		center for cancer research
cda 开始学习		confidential disclosure agreement
cdash 开始学习		clinical data acquisition standards harmonization
cder 开始学习		center for drug evaluation and research
cdm 开始学习		clinical data management
cdms 开始学习		clinical data management system
cds 开始学习		clinical data system
cdus 开始学习		clinical data updated system
cebk 开始学习		centralna ewidencja badań klinicznych
cec 开始学习		central ethics committee
cfr 开始学习		code of federal regulations
cioms 开始学习		council for international organization of medical sciences
cmax 开始学习		maximum plazma concentration
cmin 开始学习		minimum plazma concentration
cmo 开始学习		contract manufacturing organization
cns 开始学习		central nervous system
coa 开始学习		clinical outcome assesment
cov 开始学习		close out visit
cr 开始学习		complete response
cra 开始学习		clinical research associate
crc 开始学习		clinical research associate
crf 开始学习		case report form
crms 开始学习		clinical research management system
cro 开始学习		clinical research organization cro
cs 开始学习		clinical significant
cso 开始学习		contract safety organization
csr 开始学习		clinical study report
ct 开始学习		computer tomography
cta 开始学习		clinical trial agreement
cta1 开始学习		clinical trial application
cta2 开始学习		clinical trial assistant
ctcae 开始学习		common terminology criteria for adverse events
ctis 开始学习		clinical trial information system
ctms 开始学习		clinical trial management system
ctrp 开始学习		clinical and translational science award
cv 开始学习		curriculum vitae
cyp 开始学习		cytochrome p450
dar 开始学习		drug or device accountability records
db 开始学习		double blindeddb
dbl 开始学习		database lock
dcf 开始学习		data clarification form
dco 开始学习		data cut off
dhhs 开始学习		department of health and human services
dm 开始学习		data management
dmc 开始学习		data monitoring committee
doa 开始学习		delegation of authority
dp 开始学习		disease progression
dsmb 开始学习		data safety monitoring board
dsmp 开始学习		data safety monitoring plan
ec 开始学习		ethics committee
ecg 开始学习		electrocardiogram
ecog 开始学习		eastern cooperative oncology group
ecrf 开始学习		electronic case report form
ectis 开始学习		European clinical trial information
edc 开始学习		electronic data capture
edv 开始学习		early discontinuation visit
ehc 开始学习		electronic health record
ema 开始学习		European medicines agency
emea 开始学习		European agency for the evaluation of medicinal products
emr 开始学习		electronic medical record
eortc 开始学习		European organization for research and treatment of cancer
eos 开始学习		end of study
ePRO 开始学习		electronic patient reported outcomes
et 开始学习		early termination
eTMF 开始学习		electronic trial master file
eudra 开始学习		European Union drug regulatory authorities
EudraCT 开始学习		European Union clinical trials database
fair 开始学习		findable accessible interoperable reusable
fda 开始学习		food and drug administration
fdf 开始学习		financial desclosure form
fpfv 开始学习		first patient first visit
fplv 开始学习		first patient last visit
fsr 开始学习		first site ready
fu 开始学习		follow up
gcp 开始学习		good clinical practice
gcrc 开始学习		general clinical research center
gdp 开始学习		good documentation practice
glp 开始学习		good laboratory practice
gmp 开始学习		good manufacturing practice
gp 开始学习		general practicioner
haq 开始学习		health assessment questionnaire
hc 开始学习		health canada
hipaa 开始学习		health insurance portability and accountability act
ib 开始学习		investigators brochure
ICD 9 开始学习		international classification of disease 9th
icf 开始学习		informed consent form
ich 开始学习		international council for harmonization
icr 开始学习		institute of clinical research
icsr 开始学习		individual case safety
ide 开始学习		investigational device exemptions
iec 开始学习		independent ethics committee
ihcra 开始学习		in house clinical associste
iit 开始学习		investigator initiated trial
imp 开始学习		investigational medicinal product
ind 开始学习		investigational new drug
ip 开始学习		investigational product
irb 开始学习		institutional review board
irt 开始学习		interactive response technology
isf 开始学习		investigator study file
itt 开始学习		intent to treat
ivrs 开始学习		interactive voice response system
iwrs 开始学习		interactive web response system
jma 开始学习		Japan medical association
lec 开始学习		local ethics committee
loa 开始学习		letter of agreement
loa 开始学习		letter of authorization
lplv 开始学习		last patient last visit
lraa 开始学习		local regulatory affairs associate
ltfu 开始学习		long term follow up
meddra 开始学习		medical dictionary for regulatory activities
mhra 开始学习		medicines and health products regulatory agency
mmHg 开始学习		millimeters of mercury
moh 开始学习		ministry of health
mp 开始学习		monitoring plan
mri 开始学习		magnetic resonance imaging
mrn 开始学习		medical record number
mtd 开始学习		maximum tolerated dose
mv 开始学习		monitoring visit
na 开始学习		not applicable
nci 开始学习		national Cancer institute
ncs 开始学习		not clinically significant
nd 开始学习		not done
nda 开始学习		non disclosure agreement
nda 开始学习		new drug application
nhs 开始学习		national health service
nhv 开始学习		Normal healthy volunteer
nih 开始学习		national institutes of health
nimp 开始学习		non investigational medicinal product
nis 开始学习		non interventional study
nlm 开始学习		national library of medicine
oct 开始学习		office of clinical trials
ohrp 开始学习		office for human research protections
osr 开始学习		outside safety report
otc 开始学习		over the counter
pa 开始学习		protocol amendment
pa 开始学习		project assistant
pass 开始学习		post authorisation safety study
pc 开始学习		protocol coordinator
pd 开始学习		pharmacodynamics
pd 开始学习		protocol deviation
pd 开始学习		protocol director
pfs 开始学习		progression free survival
pft 开始学习		pulmonary function test
pgt 开始学习		pharmacogenetics
pgx 开始学习		pharmacogenomics
phi 开始学习		protected health information
pi 开始学习		principal investigator
pip 开始学习		paediatric investigation plan
pk 开始学习		pharmacokinetic
pl 开始学习		project lead
pm 开始学习		project manager
pma 开始学习		pre market approval
pms 开始学习		t marketing surveillance
poa 开始学习		power of attorney
pp 开始学习		per protocol
pr 开始学习		partial response
pr 开始学习		pulse rate
prmc 开始学习		protocol review and monitoring committee
prms 开始学习		otocol review and monitoring system
pro 开始学习		patient reported outcome
psur 开始学习		periodic safety update report
pv 开始学习		pharmacovigilance
qa 开始学习		quality assurance
qc 开始学习		quality control
qct 开始学习		qualifying clinical trial
ql 开始学习		quality of life
r&d 开始学习		research and development
ra 开始学习		research authority
rbm 开始学习		risk based monitoring
rca 开始学习		root cause analysis
rct 开始学习		randomised clinical trial
RDC 开始学习		emote data capture
rde 开始学习		remote data entry
recist 开始学习		response evaluation criteria in solid timors
rfp 开始学习		request for proposal
rmv 开始学习		remote monitoring visit
rtms 开始学习		randomization and trial supply management
sadr 开始学习		suspected adverse drug reaction
sae 开始学习		serious adverse event
safe 开始学习		statistical acess for everyone
sas 开始学习		statisticsl analysis system
sc 开始学习		study coordinator
scr 开始学习		screening
sd 开始学习		source data
sdr 开始学习		sourve document review
SDV 开始学习		Source data verification
sev 开始学习		ite evaluation list
sif 开始学习		site investigator file
siv 开始学习		site initiation visit
sm 开始学习		substantial modification
sme 开始学习		ssibject matter expert
smo 开始学习		site management organization
SmPC 开始学习		summary of product characteristics
smv 开始学习		site monitoring visit
soc 开始学习		standard of care
soe 开始学习		schedule of events
sop 开始学习		standard operating procedure
spores 开始学习		specialized programs for research excellence
sr 开始学习		significant risk
srb 开始学习		scientific review board
SRC 开始学习		scientific review committee
suae 开始学习		serious unaxpected adverse event
susar 开始学习		suspected unexpexted serious adverse reaction
svt 开始学习		subject visit template
tc 开始学习		tele conference
tmf 开始学习		trial master file
tmo 开始学习		trial management organization
ttp 开始学习		time to progression
uade 开始学习		unanticipated adverse device effect
uadr 开始学习		unexpected adverse drug reaction
urlp 开始学习		urząd rejestracji produktów leczniczych wyrobów medycznych i produktów biobójczych
vhp 开始学习		voluntary harmonization procedure
wbc 开始学习		White blood cell count
who 开始学习		world health organization
wl 开始学习		warning letter
wocbp 开始学习		woman of child bearing potential

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