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  Term Synonyms Abbreviation Project Category
regulatory authority RA i~HD, UNICOM
marketing authorisation medicinal product authorisation MA OpenMedicine, concePTION, UNICOM, Gravitate-Health, i~HD
medicinal product authorisation marketing authorisation OpenMedicine, concePTION, UNICOM, Gravitate-Health, i~HD
pharmaceutical product OpenMedicine, UNICOM, i~HD
identifier ID i~HD, OpenMedicine, UNICOM
international non-proprietary name INN OpenMedicine, concePTION, UNICOM, i~HD Regulatory
medicinal product identifier MPID OpenMedicine, UNICOM, i~HD
marketing authorisation holder MAH OpenMedicine, concePTION, UNICOM, Gravitate-Health, i~HD
packaged medicinal product OpenMedicine, UNICOM, i~HD
eDispensing eDispensation eD OpenMedicine, concePTION, UNICOM, Gravitate-Health, i~HD, XpanDH, xShare Information and communication technology
ePrescription electronic prescription eP OpenMedicine, UNICOM, concePTION, Gravitate-Health, i~HD, XpanDH, xShare Information and communication technology
patient summary PS OpenMedicine, UNICOM, Gravitate-Health, i~HD, XpanDH
controlled vocabulary CV OpenMedicine, UNICOM, i~HD
dose form dosage form, pharmaceutical dose form OpenMedicine, UNICOM, i~HD
dosage form dose form, pharmaceutical dose form OpenMedicine, UNICOM, i~HD
pharmaceutical dose form dose form, dosage form PDF OpenMedicine, UNICOM, i~HD
global trade item number GTIN OpenMedicine, UNICOM, i~HD
investigational medicinal product IMP OpenMedicine, concePTION, UNICOM, i~HD Clinical trials, Regulatory
adverse drug reaction ADR OpenMedicine, UNICOM, Gravitate-Health, i~HD Healthcare, Pharmacovigilance
healthcare professional health care professional HCP OpenMedicine, UNICOM, i~HD
pharmaceutical product identifier PhPID OpenMedicine, UNICOM, i~HD, xShare
pharmacovigilance PhV OpenMedicine, concePTION, UNICOM, i~HD Pharmacokinetics, Pharmacovigilance
unique device identifier UDI OpenMedicine, UNICOM, concePTION, i~HD Regulatory
investigational medicinal product identifier IMPID OpenMedicine, UNICOM, i~HD
summary of product characteristics SPC, SmPC OpenMedicine, concePTION, UNICOM, Gravitate-Health, i~HD Regulatory
route of administration RoA OpenMedicine, UNICOM, i~HD
medicines regulatory agency OpenMedicine, UNICOM, i~HD
national contact point for eHealth NCPeH OpenMedicine, UNICOM, i~HD, XpanDH, xShare
medicinal product dictionary system medicinal product dictionary MPD OpenMedicine, UNICOM, i~HD
molecular weight MW OpenMedicine, i~HD, UNICOM
clinical decision support system clinical decision support CDSS OpenMedicine, UNICOM, i~HD Healthcare, Information and communication technology
electronic health record-system functional model EHR-S FM OpenMedicine, UNICOM, i~HD
unified modeling language UML OpenMedicine, i~HD, UNICOM
uniform resource locator URL OpenMedicine, i~HD, UNICOM
object identifier OID OpenMedicine, UNICOM, i~HD
unified code for units of measure UCUM OpenMedicine, UNICOM, i~HD
British approved name BAN OpenMedicine, i~HD, UNICOM
European pharmacopoeia EP OpenMedicine, i~HD, UNICOM
Japanese accepted names JAN OpenMedicine, i~HD, UNICOM
adverse event OpenMedicine, concePTION, i~HD, UNICOM Medicines
active pharmaceutical ingredient active ingredient, active substance API OpenMedicine, UNICOM, concePTION, i~HD Medicines
manufacturer OpenMedicine, UNICOM, i~HD
anatomical therapeutic chemical anatomical therapeutic chemical classification ATC OpenMedicine, UNICOM, concePTION, i~HD Medicines
electronic prescription ePrescription EP OpenMedicine, UNICOM, concePTION, Gravitate-Health, i~HD, xShare
anatomical therapeutic chemical classification anatomical therapeutic chemical ATC UNICOM, OpenMedicine, concePTION, i~HD Medicines
medicinal product batch identifier BAID UNICOM, OpenMedicine, i~HD
biomedical research integrated domain group model BRIDG UNICOM, i~HD Clinical trials
clinical document architecture CDA UNICOM, i~HD
chemistry manufacturing and control CMC UNICOM, i~HD Medicines
data carrier identifier DCID UNICOM, i~HD
European Directorate for the Quality of Medicines & HealthCare EDQM UNICOM, OpenMedicine, Gravitate-Health, i~HD
European economic area EEA UNICOM, i~HD
European health data & evidence network EHDEN UNICOM, i~HD
smart open services for European patients epSOS UNICOM, i~HD
European surveillance of antibiotic consumption ESAC UNICOM, i~HD
health care professional healthcare professional HCP UNICOM, OpenMedicine, i~HD
investigational medicinal product batch identifier IBAID UNICOM, OpenMedicine, i~HD
international council for harmonisation of technical requirements for pharmaceuticals for human use international conference on harmonisation, international council for harmonisation ICH UNICOM, i~HD, xShare
international consortium for health outcome measurement ICHOM UNICOM, i~HD
international classification of primary care ICPC UNICOM, i~HD
individual case safety report ICSR UNICOM, OpenMedicine, Gravitate-Health, i~HD
International Medical Devices Regulators Forum IMDRF UNICOM, OpenMedicine, i~HD
investigational medicinal product package identifier IPCID UNICOM, OpenMedicine, i~HD
international patient summary IPS UNICOM, Gravitate-Health, i~HD, xShare
multi-market pack MMP UNICOM, i~HD
national trade item number NTIN UNICOM, i~HD
observational health data sciences and informatics OHDSI UNICOM, i~HD, xShare
object management group OMG UNICOM, i~HD
observational medical outcomes partnership OMOP UNICOM, i~HD, xShare
medicinal product package identifier PCID UNICOM, OpenMedicine, i~HD
national patient-centred clinical research network PCORnet UNICOM, i~HD
stock keeping unit SKU UNICOM, i~HD
single-market pack SMP UNICOM, i~HD
SNOMED clinical terms SNOMED CT UNICOM, Gravitate-Health, i~HD, xShare
World Health Organization WHO UNICOM, OpenMedicine, i~HD, xShare
WHO drug dictionary WHO-DD UNICOM, i~HD
extended EudraVigilance medicinal product dictionary XEVMPD UNICOM, i~HD
therapeutic moiety TM UNICOM, i~HD
absorption concePTION, i~HD Biology
access control concePTION, i~HD, AIDAVA Information governance
accuracy concePTION, i~HD Statistics
adaptive design concePTION, i~HD Clinical trials
adjuvant concePTION, i~HD Medicines
advanced therapy medicinal products ATMP concePTION, i~HD Medicines
adverse drug event ADE concePTION, UNICOM, i~HD Pharmacokinetics, Pharmacovigilance
adverse effect concePTION, i~HD Pharmacokinetics, Pharmacovigilance
aetiology concePTION, i~HD Biology
aggregated data concePTION, i~HD, AIDAVA Information governance
allocation concealment concePTION, i~HD Clinical trials
alternative hypothesis concePTION, i~HD Clinical trials
anonymisation concePTION, i~HD, AIDAVA Information governance
anonymised data concePTION, Gravitate-Health, i~HD, AIDAVA Information governance
antenatal care concePTION, i~HD Maternity
antibody AB concePTION, i~HD Biology
antigen concePTION, i~HD Biology
architecture concePTION, i~HD, AIDAVA Information and communication technology
area under the curve AUC concePTION, i~HD Statistics
arm concePTION, i~HD Clinical trials
artificial intelligence AI concePTION, Gravitate-Health, i~HD, AIDAVA, xShare Information and communication technology
attestation concePTION, i~HD, AIDAVA Information governance
attrition concePTION, i~HD Clinical trials
auditability concePTION, i~HD, AIDAVA Information governance
autologous concePTION, i~HD Biology
baseline assessments concePTION, i~HD Clinical trials
baseline data concePTION, i~HD Clinical trials
beneficence concePTION, i~HD Medicines
benefit-risk assessment concePTION, i~HD Regulatory
bias concePTION, i~HD Clinical trials
big data concePTION, i~HD, AIDAVA Information and communication technology
binary endpoint concePTION, i~HD Clinical trials
bioassay concePTION, i~HD Biology
biobank concePTION, i~HD Clinical trials
bioequivalence concePTION, i~HD Clinical trials
bioequivalence study concePTION, i~HD Clinical trials
biologic medicine biopharmaceutical concePTION, i~HD Medicines
biopharmaceutical biologic medicine concePTION, i~HD Medicines
biomarker concePTION, i~HD Biology
biometric data concePTION, i~HD, AIDAVA Information governance
biosimilar medicine concePTION, i~HD Medicines
biotechnology concePTION, i~HD Medicines
biotransformation concePTION, i~HD Medicines
birth weight concePTION, i~HD Maternity
blinding concePTION, i~HD Clinical trials
branded medicines concePTION, i~HD Medicines
breast milk exposure concePTION, i~HD Pharmacokinetics, Pharmacovigilance
breastfeeding concePTION, i~HD Maternity
budget impact concePTION, i~HD Regulatory
carcinogenicity studies concePTION, i~HD Clinical trials
care plan concePTION, i~HD Healthcare
case control studies concePTION, i~HD Clinical trials
case report form concePTION, i~HD Clinical trials
centralised procedure CP concePTION, i~HD Regulatory
childbearing age concePTION, i~HD Maternity
chronic condition concePTION, i~HD Medicines
class effect concePTION, i~HD Pharmacokinetics, Pharmacovigilance
clearance concePTION, i~HD Medicines
clinical effectiveness concePTION, i~HD Regulatory
clinical efficacy concePTION, i~HD Regulatory
clinical information concePTION, i~HD, AIDAVA Healthcare
clinical phase concePTION, i~HD Clinical trials
clinical process concePTION, i~HD Healthcare
clinical study report CSR concePTION, i~HD Clinical trials
clinicaltrials.gov concePTION, i~HD Clinical trials
cloud computing concePTION, i~HD, AIDAVA Information and communication technology
coefficient of variation CV concePTION, i~HD Statistics
cohort studies concePTION, i~HD Clinical trials
combined advanced-therapy medicines concePTION, i~HD Medicines
Committee for Medicinal Products for Human Use CHMP concePTION, i~HD Medicines
common technical document CTD concePTION, i~HD Regulatory
compassionate use concePTION, i~HD Regulatory
computational model concePTION, i~HD Statistics
concomitant concePTION, i~HD Medicines
confidence interval concePTION, i~HD Statistics
confidentiality concePTION, i~HD, AIDAVA Information governance
confirmatory studies concePTION, i~HD Clinical trials
confounder concePTION, i~HD Clinical trials
confounding variable concePTION, i~HD Statistics
congenital abnormality congenital malformation concePTION, i~HD Pharmacokinetics, Pharmacovigilance
congenital malformation congenital abnormality concePTION, i~HD Pharmacokinetics, Pharmacovigilance
congenital anomaly concePTION, i~HD Pharmacokinetics, Pharmacovigilance
consent concePTION, i~HD, AIDAVA Information governance
consent (assumed) assumed consent concePTION, i~HD, AIDAVA Information governance
assumed consent consent (assumed) concePTION, i~HD, AIDAVA Information governance
consent (explicit) explicit consent concePTION, i~HD, AIDAVA Information governance
explicit consent consent (explicit) concePTION, i~HD, AIDAVA Information governance
consent (implied) implied consent concePTION, i~HD, AIDAVA Information governance
implied consent consent (implied) concePTION, i~HD, AIDAVA Information governance
continuity of care concePTION, i~HD Healthcare
continuous endpoint concePTION, i~HD Clinical trials
contract research organisation CRO concePTION, i~HD Clinical trials
cost effectiveness concePTION, i~HD Regulatory
covariance concePTION, i~HD Statistics
covariate concePTION, i~HD Statistics
cross-sectional study concePTION, i~HD Clinical trials
cybersecurity concePTION, Gravitate-Health, i~HD, AIDAVA Information and communication technology
cytotoxicity concePTION, i~HD Pharmacokinetics, Pharmacovigilance
Data and Safety Monitoring Board DSMB concePTION, i~HD Clinical trials
data controller controller concePTION, Gravitate-Health, i~HD, AIDAVA Information governance
controller data controller concePTION, Gravitate-Health, i~HD, AIDAVA Information governance
data destruction concePTION, i~HD, AIDAVA Information governance
data dictionary concePTION, i~HD, AIDAVA Information and communication technology
data element concePTION, i~HD, AIDAVA Information governance
data exclusivity concePTION, i~HD Regulatory
data linkage concePTION, i~HD, AIDAVA Information governance
data model concePTION, i~HD, AIDAVA Information governance
data processor concePTION, Gravitate-Health, i~HD, AIDAVA Information governance
data sharing concePTION, i~HD, AIDAVA Information governance
data sharing agreement concePTION, i~HD, AIDAVA Information governance
data subject concePTION, i~HD, AIDAVA Information governance
database concePTION, i~HD, AIDAVA Information and communication technology
deep learning DL concePTION, i~HD, AIDAVA Information and communication technology
degradants concePTION, i~HD Medicines
determinant concePTION, i~HD Statistics
development safety update report DSUR concePTION, i~HD Regulatory
developmental and reproductive toxicity DART concePTION, i~HD Pharmacokinetics, Pharmacovigilance
digital health literacy concePTION, i~HD, AIDAVA Information and communication technology
directive concePTION, i~HD Regulatory
disability-adjusted life year DALY concePTION, i~HD Regulatory
disclose concePTION, i~HD, AIDAVA Information governance
disclosure control concePTION, i~HD, AIDAVA Information governance
disease burden concePTION, i~HD Regulatory
dosage concePTION, i~HD Medicines
dosage forms concePTION, i~HD Medicines
dosage regimen concePTION, i~HD Medicines
double blind concePTION, i~HD Statistics
drug concePTION, UNICOM, i~HD Medicines
drug candidate concePTION, i~HD Medicines
Drug Information Association DIA concePTION, i~HD Medicines
drug tolerance concePTION, i~HD Medicines
ectopic pregnancy concePTION, i~HD Maternity
Effective Concentration 50 (EC50) and Inhibition Concentration 50 (IC50) EC50 & IC50 concePTION, i~HD Pharmacokinetics, Pharmacovigilance
effectiveness concePTION, i~HD Regulatory
efficacy concePTION, i~HD Regulatory
efficiency concePTION, i~HD Regulatory
elective abortion concePTION, i~HD Maternity
electronic health record architecture concePTION, i~HD, AIDAVA Information and communication technology
electronic health record system concePTION, UNICOM, i~HD, AIDAVA Information and communication technology
electronic product information ePI concePTION, i~HD Regulatory
eligibility concePTION, i~HD Clinical trials
embryo concePTION, i~HD Maternity
embryogenesis concePTION, i~HD Biology
encryption concePTION, i~HD, AIDAVA Information and communication technology
endpoint concePTION, i~HD Clinical trials
engagement concePTION, i~HD Healthcare
epigenetics concePTION, i~HD Biology
epigenomics concePTION, i~HD Biology
EUnetHTA concePTION, i~HD Regulatory
EuroBioBank concePTION, i~HD Clinical trials
European public assessment report EPAR concePTION, i~HD Regulatory
evidence-based medicine EBM concePTION, i~HD Medicines
exclusion criteria concePTION, i~HD Clinical trials
exploratory trials concePTION, i~HD Clinical trials
extractables concePTION, i~HD Medicines
foetal death intrauterine death concePTION, i~HD Maternity
intrauterine death foetal death concePTION, i~HD Maternity
foetotoxic effect concePTION, i~HD Pharmacokinetics, Pharmacovigilance
foetus fetus concePTION, i~HD Maternity
fetus foetus concePTION, i~HD Maternity
food and drug administration concePTION, i~HD Medicines
formulation concePTION, i~HD Medicines
gene mutation concePTION, i~HD Biology
gene therapy concePTION, i~HD Biology
general data protection regulation GDPR concePTION, UNICOM, Gravitate-Health, i~HD, AIDAVA, XpanDH, xShare Information governance
general practitioner GP concePTION, UNICOM, i~HD, XpanDH, xShare Healthcare
genetic data concePTION, i~HD, AIDAVA Information governance
genetic data concePTION, i~HD Information governance
genetically modified organism GMO concePTION, i~HD Biology
genome concePTION, i~HD Biology
genome-wide association study GWAS concePTION, i~HD Clinical trials
genome-wide inferred study GWIS concePTION, i~HD Clinical trials
genomic marker concePTION, i~HD Biology
genotoxicity study concePTION, i~HD Pharmacokinetics, Pharmacovigilance
genotoxin concePTION, i~HD Biology
genotype concePTION, i~HD Biology
genotyping concePTION, i~HD Biology
gestational age Trimester concePTION, i~HD Maternity
gold standard concePTION, i~HD Biology
Good Clinical Practice GCP concePTION, i~HD Clinical trials
Good Distribution Practice GDP concePTION, i~HD Regulatory
Good Laboratory Practice GLP concePTION, i~HD Clinical trials
Good Manufacturing Practice GMP concePTION, i~HD Regulatory
Good Pharmacovigilance Practices GVP concePTION, UNICOM, i~HD Pharmacokinetics, Pharmacovigilance
group sequential design concePTION, i~HD Clinical trials
guarantee-time bias concePTION, i~HD Clinical trials
half life concePTION, i~HD Medicines
hard endpoint concePTION, i~HD Medicines
hazard ratio concePTION, i~HD Statistics
Heads of Medicines Agencies HMA concePTION, UNICOM, i~HD Medicines
health information concePTION, i~HD, AIDAVA Information and communication technology
health technology assessment HTA concePTION, i~HD Regulatory
health-related quality of life HRQoL concePTION, i~HD Regulatory
healthcare concePTION, i~HD Healthcare
healthcare activity concePTION, i~HD Healthcare
healthcare provider organisation healthcare provider concePTION, UNICOM, i~HD Healthcare
healthcare provider healthcare provider organisation concePTION, UNICOM, i~HD Healthcare
herd immunity concePTION, i~HD Medicines
high performance liquid chromatography HPLC concePTION, i~HD Pharmacokinetics, Pharmacovigilance
human biological sample concePTION, i~HD, AIDAVA Information governance
human mammary epithelial cells HMECs concePTION, i~HD Biology
idiosyncratic drug reaction concePTION, i~HD Medicines
immunogenic concePTION, i~HD Medicines
immunotoxicity concePTION, i~HD Pharmacokinetics, Pharmacovigilance
in silico concePTION, i~HD Pharmacokinetics, Pharmacovigilance
in utero concePTION, i~HD Maternity
in vitro concePTION, i~HD Pharmacokinetics, Pharmacovigilance
in vitro to in vivo extrapolation IVIVE concePTION, i~HD Pharmacokinetics, Pharmacovigilance
in vivo concePTION, i~HD Pharmacokinetics, Pharmacovigilance
incidental finding concePTION, i~HD, AIDAVA Information governance
indication concePTION, i~HD Medicines
induced abortion concePTION, i~HD Maternity
information governance concePTION, i~HD Information governance
information governance IG concePTION, i~HD, AIDAVA Information governance
information model concePTION, i~HD, AIDAVA Information and communication technology
integrated care concePTION, i~HD Healthcare
integrity concePTION, i~HD, AIDAVA Information governance
intention-to-treat ITT concePTION, i~HD Clinical trials
interim analysis concePTION, i~HD Clinical trials
intermediate endpoint concePTION, i~HD Clinical trials
internal validity concePTION, i~HD Clinical trials
international conference on harmonisation international council for harmonisation of technical requirements for pharmaceuticals for human use, international council for harmonisation ICH concePTION, UNICOM, i~HD, xShare Medicines
international council for harmonisation international council for harmonisation of technical requirements for pharmaceuticals for human use, international conference on harmonisation ICH concePTION, UNICOM, i~HD, xShare Regulatory
International Organisation for Standardization ISO concePTION, OpenMedicine, UNICOM, i~HD, XpanDH, xShare
Internet of Things IoT concePTION, i~HD, AIDAVA Information and communication technology
interventional study concePTION, i~HD Clinical trials
intrauterine growth retardation small for gestational age IUGR, SGA concePTION, i~HD Maternity
small for gestational age intrauterine growth retardation concePTION, i~HD Maternity
intravenous concePTION, i~HD Medicines
Investigational Medicinal Product Dossier IMPD concePTION, i~HD Clinical trials
knowledge model concePTION, i~HD, AIDAVA Information and communication technology
lactation concePTION, i~HD Maternity
lead-time bias concePTION, i~HD Clinical trials
Learning Health System concePTION, i~HD Healthcare
legally authorised representative LAR concePTION, i~HD Regulatory
life years LY concePTION, i~HD Clinical trials
lifetime prevalence LTP concePTION, i~HD Clinical trials
limit of detection LOD concePTION, i~HD Pharmacokinetics, Pharmacovigilance
limits of quantification LOQ concePTION, i~HD Pharmacokinetics, Pharmacovigilance
lipophilicity concePTION, i~HD Pharmacokinetics, Pharmacovigilance
live birth concePTION, i~HD Maternity
log-rank test concePTION, i~HD Statistics
low birth weight baby concePTION, i~HD Maternity
low-intervention clinical trial concePTION, i~HD Clinical trials
market exclusivity concePTION, i~HD Regulatory
marketing authorisation application MAA concePTION, UNICOM, i~HD Medicines
mass spectrometry MS concePTION, i~HD Pharmacokinetics, Pharmacovigilance
mathematical model concePTION, i~HD Pharmacokinetics, Pharmacovigilance
maximum tolerated dose MTD concePTION, i~HD Medicines
mediator variable concePTION, i~HD Statistics
medical data concePTION, i~HD, AIDAVA Information governance
medical technology assessment MTA concePTION, i~HD Clinical trials
medication error concePTION, i~HD Medicines
medication list concePTION, i~HD Medicines
medicine concePTION, i~HD Medicines
medicine distribution drug distribution concePTION, i~HD Pharmacokinetics, Pharmacovigilance
drug distribution medicine distribution concePTION, i~HD Pharmacokinetics, Pharmacovigilance
medicine model structure drug model structure concePTION, i~HD Pharmacokinetics, Pharmacovigilance
drug model structure medicine model structure concePTION, i~HD Pharmacokinetics, Pharmacovigilance
medicine specific parameters drug specific parameters concePTION, i~HD Pharmacokinetics, Pharmacovigilance
drug specific parameters medicine specific parameters concePTION, i~HD Pharmacokinetics, Pharmacovigilance
medicine transfer drug transfer concePTION, i~HD Pharmacokinetics, Pharmacovigilance
drug transfer medicine transfer concePTION, i~HD Pharmacokinetics, Pharmacovigilance
medicines list medicines formulary concePTION, i~HD Medicines
medicines formulary medicines list concePTION, i~HD Medicines
medicines management concePTION, i~HD Medicines
medicines monitoring drug monitoring concePTION, i~HD Medicines
drug monitoring medicines monitoring concePTION, i~HD Medicines
medicines optimisation concePTION, i~HD Medicines
meta-analysis concePTION, i~HD Statistics
metabolome concePTION, i~HD Biology
microarray concePTION, i~HD Biology
milk-to-plasma ratio M/P ratio concePTION, i~HD Pharmacokinetics, Pharmacovigilance
minimal anticipated biological effect level MABEL concePTION, i~HD Medicines
miscarriage spontaneous abortion concePTION, i~HD Maternity
spontaneous abortion miscarriage concePTION, i~HD Maternity
mobile health mHealth concePTION, i~HD, AIDAVA Information and communication technology
mHealth mobile health concePTION, i~HD, AIDAVA Information and communication technology
moderator variable concePTION, i~HD Statistics
molecular biomarker concePTION, i~HD Biology
multi-arm multi-stage MAMS concePTION, i~HD Clinical trials
multiplicity concePTION, i~HD Clinical trials
mutual recognition procedure MRP concePTION, UNICOM, i~HD Regulatory
neonatal physiological factors concePTION, i~HD Pharmacokinetics, Pharmacovigilance
new drug application NDA concePTION, UNICOM, i~HD Regulatory
new molecular entity NME concePTION, i~HD Medicines
no observed adverse effect level NOAEL concePTION, i~HD Clinical trials
non-clinical testing concePTION, i~HD Clinical trials
non-interventional observational study concePTION, i~HD Clinical trials
non-maleficence concePTION, i~HD Medicines
non-randomised trial concePTION, i~HD Clinical trials
null hypothesis concePTION, i~HD Statistics
number-needed-to-treat NNT concePTION, i~HD Clinical trials
observational study concePTION, i~HD Clinical trials
observer bias concePTION, i~HD Clinical trials
observer-reported outcome ObsRO concePTION, i~HD Clinical trials
off label use concePTION, i~HD Medicines
off-label use concePTION, i~HD Regulatory
Official Medicines Control Laboratory OMCL concePTION, i~HD Regulatory
organisation concePTION, i~HD, AIDAVA Information and communication technology
orphan designation concePTION, i~HD Regulatory
overdose concePTION, i~HD Medicines
p-value concePTION, i~HD Regulatory
package insert concePTION, i~HD Medicines
parameter concePTION, i~HD Statistics
parenteral concePTION, i~HD Medicines
passive surveillance concePTION, i~HD Clinical trials
pathogen concePTION, i~HD Biology
patient concePTION, UNICOM, i~HD Healthcare
patient harm concePTION, i~HD Healthcare
patient registry concePTION, i~HD Clinical trials
patient years concePTION, i~HD Statistics
patient-reported outcome PRO concePTION, i~HD Clinical trials
patient reported outcome measures PROMs concePTION, UNICOM, i~HD Clinical trials
pbpk platform concePTION, i~HD Pharmacokinetics, Pharmacovigilance
per protocol analysis concePTION, i~HD Regulatory
performance-linked access system concePTION, i~HD Pharmacokinetics, Pharmacovigilance
period of exclusivity concePTION, i~HD Regulatory
periodic benefit risk evaluation report PBRER concePTION, i~HD Regulatory
periodic safety update report PSUR concePTION, i~HD Regulatory
persisted concePTION, i~HD, AIDAVA Information and communication technology
person identification concePTION, i~HD, AIDAVA Information governance
personal data concePTION, Gravitate-Health, i~HD, AIDAVA Information governance
personal health record concePTION, i~HD, AIDAVA Information and communication technology
personalised medicine PM concePTION, i~HD Biology
perturbation concePTION, i~HD, AIDAVA Information governance
pharmacodynamics PD concePTION, i~HD Pharmacokinetics, Pharmacovigilance
pharmacoepidemiology concePTION, i~HD Biology
pharmacogenetics concePTION, i~HD Biology
pharmacogenomics PG concePTION, i~HD Biology
pharmacokinetic study concePTION, i~HD Clinical trials
pharmacokinetics PK concePTION, i~HD Pharmacokinetics, Pharmacovigilance
pharmacology concePTION, i~HD Biology
pharmacopoeia concePTION, i~HD Medicines
Phase 0 Trials concePTION, i~HD Clinical trials
Phase I Trials concePTION, i~HD Clinical trials
Phase II Trials concePTION, i~HD Clinical trials
Phase III Trials concePTION, i~HD Clinical trials
Phase IV Trials concePTION, i~HD Clinical trials
physiology-based pharmacokinetic models physiologically-based toxicokinetic models PBPK, PBTK concePTION, i~HD Pharmacokinetics, Pharmacovigilance
physiologically-based toxicokinetic models physiology-based pharmacokinetic models concePTION, i~HD Pharmacokinetics, Pharmacovigilance
pivotal study concePTION, i~HD Clinical trials
PK-Sim® concePTION, i~HD Pharmacokinetics, Pharmacovigilance
placebo concePTION, i~HD Clinical trials
placebo-controlled concePTION, i~HD Clinical trials
plasma concePTION, i~HD Biology
policy concePTION, i~HD, AIDAVA Information governance
polymerase chain reaction PCR concePTION, i~HD Biology
population concePTION, i~HD Clinical trials
population pharmacokinetics concePTION, i~HD Pharmacokinetics, Pharmacovigilance
post authorisation safety study PASS concePTION, i~HD Clinical trials
post marketing concePTION, i~HD Regulatory
post-authorisation efficacy study PAES concePTION, i~HD Regulatory
post-marketing surveillance study PMS concePTION, i~HD Regulatory
power concePTION, i~HD Statistics
pre-embryo concePTION, i~HD Maternity
predictive genetic test concePTION, i~HD Regulatory
predictive medicine concePTION, i~HD Medicines
predictive performance of medicine model predictive performance of drug model concePTION, i~HD Pharmacokinetics, Pharmacovigilance
predictive performance of drug model predictive performance of medicine model concePTION, i~HD Pharmacokinetics, Pharmacovigilance
pregnancy outcome concePTION, i~HD Maternity
premature (baby) preterm baby concePTION, i~HD Maternity
preterm baby premature (baby) concePTION, i~HD Maternity
prescribe concePTION, i~HD Medicines
prevalence concePTION, i~HD Statistics
preventable concePTION, i~HD Pharmacokinetics, Pharmacovigilance
preventable patient harm concePTION, i~HD Pharmacokinetics, Pharmacovigilance
privacy concePTION, i~HD, AIDAVA Information governance
prn PRN concePTION, i~HD Medicines
process concePTION, i~HD, AIDAVA Information and communication technology
proof of concept POC concePTION, i~HD Clinical trials
proof of mechanism POM concePTION, i~HD Clinical trials
prophylactic vaccine concePTION, i~HD Medicines
prospective cohort study concePTION, i~HD Clinical trials
prospective data collection concePTION, i~HD, AIDAVA Information governance
prospective meta-analysis concePTION, i~HD Clinical trials
proteome concePTION, i~HD Biology
proteomic marker concePTION, i~HD Biology
proteomics concePTION, i~HD Biology
pseudonym concePTION, i~HD, AIDAVA Information governance
pseudonymisation concePTION, i~HD, AIDAVA Information governance
pseudonymised data concePTION, i~HD, AIDAVA Information governance
public health concePTION, UNICOM, i~HD Healthcare
public interest concePTION, i~HD Healthcare
qualitative study concePTION, i~HD Clinical trials
quality control QC concePTION, i~HD Clinical trials
quality of life QoL concePTION, i~HD Regulatory
quality-adjusted life year QALY concePTION, i~HD Regulatory
quantitative study concePTION, i~HD Clinical trials
quasi-randomised trial concePTION, i~HD Clinical trials
randomisation concePTION, i~HD Clinical trials
randomised clinical trial concePTION, i~HD Clinical trials
randomised controlled trial RCT concePTION, i~HD Clinical trials
randomised participants concePTION, i~HD Clinical trials
rare disease concePTION, i~HD Biology
re-identification concePTION, i~HD, AIDAVA Information governance
real word evidence RWE concePTION, Gravitate-Health, i~HD, AIDAVA Information and communication technology
real world data RWD concePTION, Gravitate-Health, i~HD, AIDAVA, xShare Information and communication technology
reassortant vaccine concePTION, i~HD Medicines
recombinant DNA rDNA concePTION, i~HD Biology
recombinant gene concePTION, i~HD Biology
recruitment concePTION, i~HD Clinical trials
relative clinical effectiveness concePTION, i~HD Regulatory
relative efficacy concePTION, i~HD Regulatory
relevance concePTION, i~HD Statistics
reliability concePTION, i~HD Statistics
remission concePTION, i~HD Biology
replacement feeding concePTION, i~HD Maternity
replacement, reduction and refinement concePTION, i~HD Pharmacokinetics, Pharmacovigilance
reproductive toxicology concePTION, i~HD Pharmacokinetics, Pharmacovigilance
repurposing concePTION, i~HD Regulatory
research concePTION, i~HD, AIDAVA Information governance
response variable concePTION, i~HD Clinical trials
retrospective case control study concePTION, i~HD Clinical trials
risk concePTION, i~HD Regulatory
risk assessment concePTION, i~HD Regulatory
risk evaluation and mitigation strategy REMS concePTION, i~HD Regulatory
risk factor concePTION, i~HD Regulatory
risk management concePTION, i~HD Regulatory
risk management plan RMP concePTION, i~HD Regulatory
risk minimisation measures concePTION, i~HD, Gravitate-Health Regulatory
robustness concePTION, i~HD Pharmacokinetics, Pharmacovigilance
safety signal concePTION, i~HD Pharmacokinetics, Pharmacovigilance
safety specification concePTION, i~HD Pharmacokinetics, Pharmacovigilance
sample size concePTION, i~HD Clinical trials
Scientific Advice Working Party SAWP concePTION, i~HD Regulatory
Scientific Advisory Group SAG concePTION, i~HD Regulatory
secondary use of data (or data re-use) concePTION, i~HD, AIDAVA Information governance
selection bias concePTION, i~HD Clinical trials
selective reporting concePTION, i~HD Clinical trials
sensitivity concePTION, i~HD Clinical trials
sensitivity concePTION, i~HD, AIDAVA Information governance
sensitivity concePTION, i~HD Pharmacokinetics, Pharmacovigilance
sensitivity analysis concePTION, i~HD Statistics
serious adverse event SAE concePTION, i~HD Pharmacokinetics, Pharmacovigilance
side effect concePTION, i~HD Pharmacokinetics, Pharmacovigilance
sign concePTION, i~HD Pharmacokinetics, Pharmacovigilance
signal concePTION, i~HD Statistics
signalling pathway concePTION, i~HD Biology
significance concePTION, i~HD Statistics
significance level concePTION, i~HD Statistics
silencing concePTION, i~HD Biology
Simcyp® concePTION, i~HD Pharmacokinetics, Pharmacovigilance
single ascending dose study SAD concePTION, i~HD Clinical trials
social care provider organisation concePTION, i~HD Healthcare
soft endpoint concePTION, i~HD Clinical trials
somatic concePTION, i~HD Biology
specificity concePTION, i~HD Statistics
sponsor concePTION, i~HD Clinical trials
spontaneous abortion concePTION, i~HD Maternity
standard concePTION, i~HD, AIDAVA Information and communication technology
standard deviation concePTION, i~HD Statistics
statistical analysis plan SAP concePTION, i~HD Clinical trials
statistical significance concePTION, i~HD Statistics
stem cell therapy concePTION, i~HD Biology
stem cells concePTION, i~HD Biology
stillbirth concePTION, i~HD Maternity
stratification concePTION, i~HD Clinical trials
stratified medicine concePTION, i~HD Biology
strong authentication concePTION, i~HD, AIDAVA Information governance
structure-activity relationships and quantitative structure-activity relationships SAR/QSAR concePTION, i~HD Pharmacokinetics, Pharmacovigilance
study participant concePTION, i~HD, AIDAVA Information governance
subject of care concePTION, i~HD Healthcare
submission concePTION, i~HD Regulatory
substances, products, organisations and referentials SPOR concePTION, UNICOM, Gravitate-Health, i~HD Medicines
sudden infant death syndrome SIDS concePTION, i~HD Maternity
Supervisory Authority concePTION, i~HD, AIDAVA Information governance
surrogate endpoint concePTION, i~HD Clinical trials
suspected unexpected serious adverse reaction SUSAR concePTION, i~HD Pharmacokinetics, Pharmacovigilance
system dependent components concePTION, i~HD Biology
t-test concePTION, i~HD Statistics
target patient population concePTION, i~HD Clinical trials
target product profile TPP concePTION, i~HD Clinical trials
targeted medicine concePTION, i~HD Medicines
teratogen concePTION, i~HD Pharmacokinetics, Pharmacovigilance
teratogenic concePTION, i~HD Pharmacokinetics, Pharmacovigilance
teratology concePTION, i~HD Pharmacokinetics, Pharmacovigilance
termination of pregnancy abortion concePTION, i~HD Maternity
abortion termination of pregnancy concePTION, i~HD Maternity
testing method concePTION, i~HD Pharmacokinetics, Pharmacovigilance
therapeutic alternatives concePTION, i~HD Medicines
third sector provider organisation concePTION, i~HD Healthcare
time-to-event endpoint TTE concePTION, i~HD Clinical trials
tolerability concePTION, i~HD Medicines
toxicity concePTION, i~HD Pharmacokinetics, Pharmacovigilance
toxicokinetics concePTION, i~HD Pharmacokinetics, Pharmacovigilance
TQTc concePTION, i~HD Clinical trials
transcriptome concePTION, i~HD Biology
transgenic concePTION, i~HD Biology
treatment emergent adverse event TEAE concePTION, i~HD Pharmacokinetics, Pharmacovigilance
treatment group concePTION, i~HD Clinical trials
trial arm concePTION, i~HD Clinical trials
trusted third party TTP concePTION, i~HD, AIDAVA Information governance
Type I error concePTION, i~HD Statistics
Type II error concePTION, i~HD Statistics
uncertainty concePTION, i~HD Statistics
United States package insert USPI concePTION, i~HD Regulatory
validation concePTION, i~HD Statistics
variable concePTION, i~HD Statistics
variance concePTION, i~HD Statistics
vector concePTION, i~HD Biology
very low birth weight (baby) concePTION, i~HD Maternity
vulnerable participants or populations concePTION, i~HD Medicines
wash out period concePTION, i~HD Clinical trials
whole genome sequencing WGS concePTION, i~HD Biology
workflow concePTION, i~HD Healthcare
Z-factor concePTION, i~HD Pharmacokinetics, Pharmacovigilance
zygote concePTION, i~HD Maternity
active substance active ingredient, active pharmaceutical ingredient concePTION, OpenMedicine, UNICOM, i~HD Medicines
audit trail concePTION, OpenMedicine, i~HD, AIDAVA Information governance
authentication concePTION, OpenMedicine, i~HD, AIDAVA Information governance
care pathway concePTION, OpenMedicine, i~HD Healthcare
data concePTION, OpenMedicine, i~HD, AIDAVA Information and communication technology
de-identification concePTION, OpenMedicine, i~HD, AIDAVA Information governance
electronic health record EHR concePTION, OpenMedicine, UNICOM, Gravitate-Health, i~HD, AIDAVA, XpanDH, xShare Information and communication technology
European Medicines Agency EMA concePTION, OpenMedicine, UNICOM, i~HD Medicines
excipient concePTION, OpenMedicine, UNICOM, i~HD Medicines
identification of medicinal products IDMP concePTION, OpenMedicine, UNICOM, Gravitate-Health, i~HD, XpanDH Medicines
inclusion criteria concePTION, OpenMedicine, i~HD Clinical trials
medication concePTION, OpenMedicine, i~HD Medicines
medicinal product MP concePTION, OpenMedicine, UNICOM, i~HD Healthcare
national competent authority national drug authority, national medicines authority NCA concePTION, OpenMedicine, UNICOM, i~HD Regulatory
national drug authority national competent authority, national medicines authority concePTION, OpenMedicine, UNICOM, i~HD Regulatory
processing concePTION, OpenMedicine, Gravitate-Health, i~HD, AIDAVA Information governance
role concePTION, OpenMedicine, i~HD, AIDAVA Information governance
serious adverse reaction serious ADR SAR concePTION, OpenMedicine, UNICOM, i~HD Pharmacokinetics, Pharmacovigilance
serious ADR serious adverse reaction concePTION, OpenMedicine, UNICOM, i~HD Pharmacokinetics, Pharmacovigilance
third party concePTION, OpenMedicine, i~HD, AIDAVA Information governance
model verification concePTION, i~HD Statistics
Spanish Medicine Agency AEMPS UNICOM, i~HD
active substance master file ASMF UNICOM, i~HD Regulatory
Federal Institute for medicines & medical devices in Germany BfArM UNICOM, i~HD
centrally authorised product CAP UNICOM, i~HD Regulatory
cross-border eHealth information services CBeHIS UNICOM, i~HD
Medicines Evaluation Board of the Netherlands CBG-MEB UNICOM, i~HD
combined pharmaceutical dose form UNICOM, i~HD
common data model CDM UNICOM, i~HD
common European submission portal CESP UNICOM, i~HD
Coordination Group for Mutual Recognition and Decentralised Procedures - Human CMDh UNICOM, i~HD
Coordination Groups for Mutual Recognition and Decentralised Procedures CMDs UNICOM, i~HD
Coordination Group for Mutual Recognition and Decentralised Procedures - Veterinary CMDv UNICOM, i~HD
database administrator DBA UNICOM, i~HD
decentralised procedure DCP UNICOM, i~HD
German substance registration system DE-SRS UNICOM, i~HD
Digital Imaging and Communications in Medicine DICOM UNICOM, i~HD
electronic application form eAF UNICOM, i~HD
European Medicines Regulatory Network EMRN UNICOM, i~HD
European risk management strategy ERMS UNICOM, i~HD
European Free Trade Association EFTA UNICOM, i~HD
European substance registration system EU-SRS UNICOM, i~HD
European Union Network Data Board EUNDB UNICOM, i~HD
European Union telematics controlled terms EUTCT UNICOM, i~HD
global substance registration system GSRS UNICOM, i~HD
hyper text transfer protocol HTTP UNICOM, i~HD
IRIS Platform UNICOM, i~HD
integrated patient management system IPMS UNICOM, i~HD
IT Directors Executive Committee ITDEC UNICOM, i~HD
Agency for Medicinal Products and Medical Devices of the Republic of Slovenia JAZMP UNICOM, i~HD Regulatory
marketing authorisation procedure MAP UNICOM, i~HD
market authorisation variation MAV UNICOM, i~HD
medical dictionary for regulatory activities MedDRA UNICOM, concePTION, Gravitate-Health, i~HD, xShare
Swedish Medical Products Agency Medical Products Agency of Sweden SEMPA UNICOM, i~HD
nationally authorised product NAP UNICOM, i~HD
National Centre for Advancing Translational Sciences NCATS UNICOM, i~HD, xShare
National Institutes of Health NIH UNICOM, i~HD
national medicines authority national competent authority, national drug authority NMA UNICOM, OpenMedicine, concePTION, i~HD
Norwegian Medicines Agency NoMA UNICOM, i~HD
national procedure NP UNICOM, i~HD
organisation management service OMS UNICOM, i~HD
prescribing and dispensing software system PDSS UNICOM, i~HD
programme for international drug monitoring PIDM UNICOM, i~HD
patient-facing mobile health application PMHA UNICOM, i~HD
referential management service RMS UNICOM, i~HD
standards knowledge management tool SKMT UNICOM, i~HD
substance management service SMS UNICOM, i~HD
State Institute for Drug Control of Czech Republic SUKL UNICOM, i~HD
Substance Validation Group SVG UNICOM, i~HD
Telematics Management Board EU Telematics Management Board TMB UNICOM, i~HD
unit of presentation UoP UNICOM, i~HD
eHealth digital service infrastructure eHDSI UNICOM, i~HD, XpanDH, xShare
member state of treatment country B UNICOM, i~HD
member state of affiliation country A UNICOM, i~HD
protection of personal data POPD UNICOM, i~HD
ethics advisory board EAB UNICOM, i~HD
Agency for Healthcare Research and Quality AHRQ UNICOM, i~HD Regulatory
primary package UNICOM, i~HD
secondary package UNICOM, i~HD
GS1 UNICOM, i~HD
application programming interface API UNICOM, Gravitate-Health, i~HD, AIDAVA Information and communication technology
European Medicines Verification Organisation EMVO UNICOM, i~HD
European Union falsified medicines directive EU-FMD UNICOM, i~HD
medicinal product dictionary medicinal product dictionary system MPD UNICOM, OpenMedicine, i~HD
Uppsala Monitoring Centre WHO-UMC UNICOM, i~HD
country A member state of affiliation UNICOM, i~HD
country B member state of treatment UNICOM, i~HD
national contact point NCP UNICOM, i~HD
eHealth UNICOM, i~HD
Medicines & Healthcare products Regulatory Agency of the United Kingdom MHRA UNICOM, i~HD
Medical Products Agency of Sweden Swedish Medical Products Agency MPA UNICOM, i~HD
fast healthcare interoperability resources FHIR UNICOM, Gravitate-Health, i~HD, AIDAVA, xShare Information and communication technology
allergen UNICOM, i~HD Healthcare
attribute UNICOM, i~HD, AIDAVA Information and communication technology
available prescription UNICOM, i~HD eDispensation, ePrescription
clinical information system UNICOM, i~HD
coding system UNICOM, i~HD
dispensed medicine UNICOM, i~HD
dispenser UNICOM, i~HD
eDispensation eDispensing eD UNICOM, i~HD, XpanDH, xShare
eHealth Network eHN UNICOM, i~HD, XpanDH, xShare
generic medicinal product UNICOM, i~HD
guideline UNICOM, i~HD
hospital information system HIS UNICOM, i~HD
master value sets catalogue MVC UNICOM, i~HD, xShare
medical record medical health record UNICOM, i~HD
medication summary UNICOM, i~HD
medicinal prescription UNICOM, i~HD
posology UNICOM, i~HD
prescriber UNICOM, i~HD
substance UNICOM, i~HD
time valid prescription UNICOM, i~HD
valid prescription UNICOM, i~HD
Federal Agency for Medicines and Health Products of Belgium AFMPS UNICOM, i~HD
Agency for Health and Food Safety in Austria AGES UNICOM, i~HD Regulatory
Agency for Food, Environmental and Occupational Health and Safety of France ANSES UNICOM, i~HD Regulatory
Clinical Data Interchange Standards Consortium CDISC UNICOM, i~HD, xShare
Republic of Estonia Agency of Medicines State Agency of Medicines of Estonia EESAM UNICOM, i~HD
clinical trial information system CTIS UNICOM, i~HD
EU Telematics Management Board Telematics Management Board EUTMB UNICOM, i~HD
Finnish Medicines Agency FIMEA UNICOM, i~HD
Agency for Medicinal Products and Medicinal Devices of Croatia HALMED UNICOM, i~HD Regulatory
Health Level Seven International HL7 UNICOM, i~HD, xShare
National Authority of Medicines and Health Products of Portugal INFARMED UNICOM, i~HD
product management services PMS UNICOM, i~HD
medical health record medical record UNICOM, i~HD
European Federation of Pharmaceutical Industries and Associations EFPIA UNICOM, concePTION, i~HD Medicines
Food and Drug Administration of the United States FDA UNICOM, concePTION, i~HD, xShare Medicines
standards developing organisation SDO UNICOM, i~HD, XpanDH, xShare
lead member state LMS UNICOM, i~HD
international nonproprietary names modified INNM UNICOM, i~HD
modified substance UNICOM, i~HD
virtual medicinal product VMP UNICOM, i~HD
virtual medicinal product group VMP Group UNICOM, i~HD
actual medicinal product AMP UNICOM, i~HD Medicines
actual medicinal product package AMPP UNICOM, i~HD Medicines
virtual therapeutic moiety VTM UNICOM, i~HD
EU Telematics UNICOM, i~HD
State Agency of Medicines of Estonia Republic of Estonia Agency of Medicines SAM UNICOM, i~HD
active ingredient active pharmaceutical ingredient, active substance concePTION, OpenMedicine, UNICOM, i~HD Pharmacokinetics, Pharmacovigilance
clinical decision support clinical decision support system CDS UNICOM, concePTION, i~HD Healthcare
over the counter medicine OTC UNICOM, concePTION, Gravitate-Health, i~HD
basis of strength substance BoSS UNICOM, i~HD Medicines
precise active ingredient substance PAI UNICOM, i~HD
evidence based medicine EBM UNICOM, i~HD
electronic medication administration record eMAR UNICOM, i~HD
technical specification TS UNICOM, i~HD
adverse event following immunisation AEFI UNICOM, i~HD Healthcare, Pharmacovigilance
chemical abstracts service CAS UNICOM, i~HD Medicines
European Commission EC UNICOM, i~HD, XpanDH, xShare
European Union EU UNICOM, i~HD, AIDAVA, XpanDH, xShare
National Health Service NHS UNICOM, i~HD
standardised drug grouping SDG UNICOM, i~HD
substance identifier SID UNICOM, i~HD
EudraVigilance EV UNICOM, i~HD
VigiBase UNICOM, i~HD
defined daily dose DDD UNICOM, i~HD Pharmacovigilance
clinical drug CD Precisely UNICOM, i~HD Medicines
dictionary of medicines and devices dm+d UNICOM, i~HD
international classification of diseases international statistical classification of diseases and health related problems ICD UNICOM, i~HD, xShare
international statistical classification of diseases and health related problems international classification of diseases ICD UNICOM, i~HD, xShare
linked open data LOD UNICOM, i~HD
medical subject headings MeSH UNICOM, i~HD
National Library of Medicine of the United States NLM UNICOM, i~HD
ministry of health MoH UNICOM, i~HD, xShare
medicinal product containing only MP-only UNICOM, i~HD
potentially inappropriate medication list PIM list UNICOM, i~HD
patient reported experience measures PREMs UNICOM, i~HD
Source Authentique des Médicaments SAM UNICOM, i~HD
unified medical language system UMLS UNICOM, i~HD
unique ingredient identifier UNII UNICOM, i~HD
communication and tracking system CTS UNICOM, i~HD
user acceptance testing UAT UNICOM, i~HD
work package WP UNICOM, i~HD, XpanDH, xShare Contractual and project management
IT system/database for drug data at EESAM SamTrack UNICOM, i~HD
pilot product list PPL UNICOM, i~HD
Federal Office for Safety in Health Care in Austria BASG UNICOM, i~HD
description of action DoA UNICOM, i~HD, XpanDH Contractual and project management
implementation guide IG UNICOM, i~HD, XpanDH
business segment of AGES medicines & medical devices agency (AGES) in Austria MEA UNICOM, i~HD
project manager PM UNICOM, i~HD
Digital Application Dataset Integration Project DADI UNICOM, i~HD
relational data model RDM UNICOM, i~HD
integrated regulatory information system iRis UNICOM, i~HD
user interface UI UNICOM, Gravitate-Health, i~HD
user experience UX UNICOM, Gravitate-Health, i~HD
WinPure UNICOM, i~HD
Health Products Regulatory Authority in Ireland HPRA UNICOM, i~HD
HPRA case management system EOLAS UNICOM, i~HD
union product database UPD UNICOM, i~HD
FIMEA's new medicines registry Saga UNICOM, i~HD
secure shell file transfer protocol SFTP UNICOM, i~HD Information and communication technology
Institute for Health and Welfare of Finland THL UNICOM, i~HD
national organisations repository of National Authority of Medicines and Health Products of Portugal GENT UNICOM, i~HD
INFARMED national repository of medicinal products GiMED UNICOM, i~HD
INFARMED national substances repository GSUB UNICOM, i~HD
International Organization for Standardization for the identification of medicinal products ISO IDMP UNICOM, i~HD
standard operating procedure SOP UNICOM, i~HD
Centre for Pharmacological Information in Belgium BCFI UNICOM, i~HD
dossiers tracking system DTS UNICOM, i~HD
INFARMED national reference data management system GDR UNICOM, i~HD
extra plus revised E + R UNICOM, i~HD
health intelligence reporting system HIRS UNICOM, i~HD
national institute for health and disability insurance in Belgium RIZIV/INAMI UNICOM, i~HD
workflow system used by the Federal Agency of Medecines and Health Products of Belgium MeSeA UNICOM, i~HD
medicinal product management MPM UNICOM, i~HD
OMS organisation identifier org-id UNICOM, i~HD
marketing authorisation holders for veterinary products VET-MAH's UNICOM, i~HD
infrastructure as a service IaaS UNICOM, i~HD
platform as a service PaaS UNICOM, i~HD, AIDAVA Information and communication technology
assessment and evaluation tools for e-service deployment in health, care and ageing ASSIST Gravitate-Health, i~HD, UNICOM Information and communication technology
semantic clinical drug SCD UNICOM, i~HD
defined daily doses per 1000 inhabitants per day DID UNICOM, i~HD
single-dose container UNICOM, i~HD Medicines
unit-dose blister UNICOM, i~HD eDispensation, ePrescription
FAIR principles Gravitate-Health, i~HD, AIDAVA, UNICOM Information governance
Connecting Europe Facility CEF UNICOM, i~HD
European Commission EC UNICOM, i~HD, AIDAVA, xShare
eHealth Member States Experts Group eHMSEG UNICOM, i~HD
EMA IDMP implementation guide V2 EMA IG V2 UNICOM, i~HD
electronic product information ePI UNICOM, i~HD
EU IDMP Implementation Guide EU IG UNICOM, i~HD
medicinal product dictionary MPD UNICOM, i~HD
pharmaceutical product PhP UNICOM, i~HD Medicines
UNICOM FHIR IDMP server UFIS UNICOM Information and communication technology
product lifecycle management portal PLM UNICOM
European Association of Hospital Pharmacists EAHP UNICOM
European Association of E-Pharmacies EAEP UNICOM
Pharmaceutical Group of the European Union PGEU UNICOM
Global IDMP Working Group GIDWG UNICOM
project coordinator PC UNICOM
project coordination committee PCC UNICOM
project coordination team PCT UNICOM
project executive committee PEC UNICOM
project management team PMT UNICOM
project officer PO UNICOM
strategy board SB UNICOM
small and medium-sized enterprises SMEs UNICOM
scientific and technical coordination office STCO UNICOM
work package leader WPL UNICOM
cost-benefit analysis CBA UNICOM
EMA common repository EMA CR UNICOM
drug information centre DIC UNICOM
European Interoperability Framework EIF UNICOM
Joint Research Centre JRC UNICOM
key performance indicator KPI UNICOM
maple language file MPL UNICOM
national repository for medicinal products in Sweden NPL UNICOM
national medicinal products registry of Croatia NRL UNICOM
portable document format PDF UNICOM
quality assurance QA UNICOM
reference data model RDM UNICOM
Swedish krona SEK UNICOM
INFARMED platform for submission of variation applications SMUH‐ALTER UNICOM
substances, products, intressent (organisation), referentials, automation SPIRA UNICOM
Shared Services of the Ministry of Health in Portugal SPMS UNICOM
Extensible Markup Language XML UNICOM
comma-separated values CSV UNICOM
electronic common technical document eCTD UNICOM
global substance identifier GSID UNICOM
integrated taxonomic information system ITIS UNICOM
kyoto encyclopedia of genes and genomes KEGG UNICOM
medicinal plant names services MPNS UNICOM
National Center for Biotechnology Information NCBI UNICOM
National Cancer Institute NCI UNICOM
substance management services identifier SMSID UNICOM
specified substance group 1 SSG1 UNICOM
substance validation group identifier SVGID, SVGID UNICOM
Uppsala Monitoring Centre substance registration system UMC-SRS UNICOM
veterinary ATC VATC UNICOM
Systematic Nomenclature of Medicine International SNOMED International UNICOM
additional listing name AL UNICOM
british pharmacopoeia BP UNICOM
dalton Da UNICOM
display name DN UNICOM
deoxyribonucleic acid DNA UNICOM
ethylenediaminetetraacetic acid EDTA UNICOM
eudravigilance medicinal product dictionary EVMPD UNICOM
Homöopathisches Arzneibuch/German Homoeopathic Pharmacopoeia HAB/GHP UNICOM
International Committee on Taxonomy of Viruses ICTV UNICOM
immunoglobulin g IGG UNICOM
inn proposed list INN PL UNICOM
inn recommended list INN RL UNICOM
International Organisation for Standardization technical specifications ISO/TS UNICOM
International Union of Pure and Applied Chemistry IUPAC UNICOM
list of prokaryotic names with standing in nomenclature LSPN UNICOM
monoclonal antibody MAB UNICOM
messenger ribonucleic acid mRNA UNICOM
european pharmacopoeia Ph. Eur. UNICOM
french pharmacopoeia Ph. Fr. UNICOM
proposed INN pINN UNICOM
recommended INN rINN UNICOM
preferred term PT UNICOM
ribonucleic acid RNA UNICOM
simplified molecular-input line-entry system SMILES UNICOM
specified substance group SSG UNICOM
scientific and technical information network STN UNICOM
tumor necrosis factor TNF UNICOM
United States US UNICOM
United States adopted name USAN UNICOM
consortium agreement CA i~HD, AIDAVA, XpanDH Contractual and project management
European health data space EHDS i~HD, AIDAVA, XpanDH, xShare Digital Service Infrastructure
Health Data Intermediary HDI i~HD, AIDAVA Healthcare
basic local alignment search tool BLAST UNICOM
javascript object notation JSON UNICOM
common specifications European EHRxF specifications i~HD, XpanDH, xShare Digital Service Infrastructure
common content specifications i~HD, XpanDH, xShare Digital Service Infrastructure
electronic health data i~HD, XpanDH, xShare Digital Service Infrastructure
priority categories of electronic health data i~HD, XpanDH, xShare
European electronic health record exchange format EEHRxF i~HD, XpanDH, xShare
electronic health record exchange format EHRxF i~HD, XpanDH, xShare
patient generated health data PGHD i~HD, XpanDH, xShare Information governance
regulator i~HD, XpanDH, xShare Regulatory
exchanging electronic health records in a common framework X-eHealth i~HD, XpanDH, xShare Digital Service Infrastructure
European EHRxF specifications common specifications i~HD, XpanDH, xShare
expanding digital health through a pan-European EHRxF-based ecosystem XpanDH i~HD, XpanDH, xShare
experimentation bubble X-Bubble i~HD, XpanDH, xShare
X-Bundle i~HD, XpanDH, xShare Digital Service Infrastructure
X-Net i~HD, XpanDH, xShare
common data element i~HD, XpanDH, xShare Digital Service Infrastructure
sandbox i~HD, xShare Digital Service Infrastructure
industry trade association national trade association i~HD, xShare Generic
industry forum i~HD, xShare
regulators forum i~HD, xShare
sustainable by design i~HD, XpanDH, xShare
health information domain HID i~HD, XpanDH, xShare
prioritised health information domain i~HD, XpanDH, xShare Digital Service Infrastructure
refined eHealth European interoperability framework ReEIF i~HD, XpanDH, xShare
extended EHR@EU data space for primary use Xt-EHR i~HD, XpanDH, xShare
MyHealth@EU i~HD, XpanDH, xShare Digital Service Infrastructure
my health space i~HD, xShare Digital Service Infrastructure
health priority focus area i~HD, XpanDH, xShare
adoption domain i~HD, XpanDH, xShare
xShare button xShare yellow button i~HD, xShare
expanding the European EHRxF to share and effectively use health data within the EHDS xShare i~HD, UNICOM
EU xShare label i~HD, xShare
European Union digital identity EUDI i~HD, xShare Digital Service Infrastructure
EUDI wallet i~HD, xShare Digital Service Infrastructure
HealthData@EU i~HD, XpanDH, xShare
Health Level Seven HL7 UNICOM
HL7 Europe Foundation HL7 Europe i~HD, XpanDH, xShare
Integrating the Healthcare Enterprise Europe IHE Europe i~HD, XpanDH, xShare
European Committee for Standardization CEN i~HD, XpanDH, xShare
Institute of Electrical and Electronics Engineers IEEE i~HD, xShare
Integrating the Healthcare Enterprise IHE i~HD, XpanDH, xShare
European health data space for primary use of electronic health data EHDS-1 i~HD, XpanDH, xShare
European health data space for secondary use of electronic health data EHDS-2 i~HD, XpanDH, xShare
FHIR Implementation Guide FHIR IG i~HD, XpanDH, xShare
coronavirus disease 2019 COVID-19 i~HD, xShare
massive open on-line course MOOC i~HD, xShare
electronic identification and trust services eIDAS i~HD, XpanDH, xShare
European CRO Federation EUCROF i~HD, xShare
clinical data acquisition standards harmonization CDASH i~HD, xShare
electronic health record systems for clinical research EHR4CR i~HD, xShare
electronic health record systems to electronic data capture EHR2EDC i~HD, xShare
population health information research infrastructure PHIRI i~HD, xShare
code supervisory body COSUP i~HD, xShare
Pharmaceuticals and Medical Devices Agency of Japan PMDA i~HD, xShare
human computer interaction HCI AIDAVA Information and communication technology
SVG substance registration system SVG-SRS UNICOM
Italian Medicines Agency AIFA UNICOM
French Agency for Safety of Medicines and Health Products ANSM UNICOM
Paul Ehrlich Institute PEI UNICOM
clinical trial information system - business intelligence system CTIS BI UNICOM
international coalition of medicines regulatory authorities ICMRA UNICOM
national trade association industry trade association NTA xShare, i~HD
Digital Single Market DSM XpanDH
Centre for Documentation and Costing of Hospital Services in Greece DRG Institute XpanDH
DRG coding guidelines in Greece EKOK XpanDH
medical procedure classification in Greece ETIP XpanDH
National Organization for Provision of Health Services in Greece EOPYY XpanDH
digital consumer health product DCHP XpanDH
research ethics committee REC XpanDH Contractual and project management
European reference network ERN XpanDH
international classification of diseases - 10th revision ICD-10 XpanDH
information and communications technology ICT XpanDH
organisation for quality assurance in health in Greece ODIPY XpanDH
Digital Health Europe round tables RT XpanDH
surgical site infection SSI XpanDH
task T UNICOM, XpanDH Contractual and project management
reporting period RP XpanDH Contractual and project management
mutual insurance mechanism MIM XpanDH Contractual and project management
grant agreement GA XpanDH Contractual and project management
artificial intelligence act AI Act XpanDH
business to business B2B XpanDH
business to consumer B2C XpanDH
business to government B2G XpanDH
cyber resilience act CRA XpanDH
cybersecurity act CSA XpanDH
data protection impact assessment DPIA XpanDH
electronic identification eID XpanDH
findable, accessible, interoperable, reusable FAIR XpanDH Information governance
EU recovery and resilience facility RRF XpanDH
Agency for Integration, Diffusion and Archive of Medical Information AIDA XpanDH
diagnosis related group DRG XpanDH
Greek medical procedure classification GMPC XpanDH
DRG system in Greece GrDRG XpanDH
cross-enterprise document sharing XDS XpanDH
dissemination, communication, outreach and exploitation plan DCOEP XpanDH Contractual and project management
dissemination, communication, outreach, and exploitation DCOE XpanDH Contractual and project management
European Health and Digital Executive Agency HaDEA XpanDH Contractual and project management
co-creation community of patients, professionals and programmers 3Cs-3Ps XpanDH
electronic health record system EHR-S XpanDH, xShare
eHDSI Operational Management Board eHOMB xShare
Joint Action Towards the European Health Data Space TEHDAS xShare
Joint Action Towards the European Health Data Space 2 TEHDAS2 xShare
xShare yellow button xShare button xShare, i~HD