→ Badania Kliniczne → Start Learning / Download MP3 Flashcards

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

Badania Kliniczne

You must sign in to write a comment

More