CDISC Glossary Terminology

Preferred Label : CDISC Glossary Terminology;

NCIt synonyms : CDISC-GLOSSARY; CDISC-GLOSS; Clinical Data Interchange Standards Consortium Glossary;

NCIt related terms : CDISC Glossary;

NCIt definition : The terminology that includes terms relevant to the Clinical Data Interchange Standards Consortium Glossary group.;

Alternative definition : CDISC-GLOSS: The terminology of the Clinical Data Interchange Standards Consortium (CDISC) glossary.;

Détails

Origin ID

C67497;

UMLS CUI

C4553192;

Semantic type(s)
- Intellectual Product [UMLS semantic type]
concept_is_in_subset
- Clinical Data Interchange Standards Consortium Terminology [NCIt concept]
subset_includes_concept
- ADROIT Electronically Generated Information Service [NCIt concept]
- Abbreviation [NCIt concept]
- Accelerated Approval [NCIt concept]
- Accrual [NCIt concept]
- Acronym [NCIt concept]
- Active Ingredient [NCIt concept]
- Active Ingredient Dose [NCIt concept]
- Active Substance [NCIt concept]
- Adaptive Design [NCIt concept]
- Additive Effect [NCIt concept]
- Adequate and Well-controlled Study [NCIt concept]
- Adherence [NCIt concept]
- Administrable Dosage Form [NCIt concept]
- Admission Criteria [NCIt concept]
- Adverse Drug Reaction [NCIt concept]
- Adverse Event [NCIt concept]
- Adverse Event Outcome [NCIt concept]
- Adverse Reaction [NCIt concept]
- Agent Administration [NCIt concept]
- Algorithm [NCIt concept]
- Alpha Error [NCIt concept]
- Amendment [NCIt concept]
- American Health Information Community [NCIt concept]
- American National Standards Institute [NCIt concept]
- Analysis [NCIt concept]
- Analysis Dataset [NCIt concept]
- Analysis Set of Subjects [NCIt concept]
- Analysis Variable [NCIt concept]
- Anonymization [NCIt concept]
- Antagonistic Effect [NCIt concept]
- Antibody [NCIt concept]
- Antigen [NCIt concept]
- Applet [NCIt concept]
- Applicable Regulatory Requirement [NCIt concept]
- Approval Document [NCIt concept]
- Arithmetic Mean [NCIt concept]
- Artificial Intelligence [NCIt concept]
- Assent Form [NCIt concept]
- Assessment [NCIt concept]
- Attributable, Legible, Contemporaneous, Original, Accurate [NCIt concept]
- Attributable, Legible, Contemporaneous, Original, Accurate Plus [NCIt concept]
- Attributable, Legible, Contemporaneous, Original, Accurate Plus Plus [NCIt concept]
- Attribution [NCIt concept]
- Audit [NCIt concept]
- Audit Certificate [NCIt concept]
- Audit Report [NCIt concept]
- Audit Trail [NCIt concept]
- Authorization [NCIt concept]
- Authorized Auxiliary Medicinal Product [NCIt concept]
- Authorized Investigational Medicinal Product [NCIt concept]
- Auxiliary Medicinal Product [NCIt concept]
- Back Translation [NCIt concept]
- Background Treatment [NCIt concept]
- Balanced Study [NCIt concept]
- Bandwidth [NCIt concept]
- Baseline Assessment [NCIt concept]
- Baseline Characteristics [NCIt concept]
- Baseline Imbalance [NCIt concept]
- Basket Trial [NCIt concept]
- Basket Trial Design [NCIt concept]
- Bayesian Approach [NCIt concept]
- Bayesian Statistics [NCIt concept]
- Best Practice [NCIt concept]
- Beta Error [NCIt concept]
- Bias [NCIt concept]
- Bioassay [NCIt concept]
- Bioavailability [NCIt concept]
- Bioequivalence [NCIt concept]
- Biological Absorption [NCIt concept]
- Biological Agent [NCIt concept]
- Biologics License Application [NCIt concept]
- Biomarker [NCIt concept]
- Biometric Signature [NCIt concept]
- Biosimilar [NCIt concept]
- Biostatistics [NCIt concept]
- Blind Review [NCIt concept]
- Blinded [NCIt concept]
- Blinded Clinical Study [NCIt concept]
- Blinded Medication [NCIt concept]
- CDISC Classifier Role [NCIt concept]
- CDISC General Observation Class [NCIt concept]
- CDISC Library [NCIt concept]
- CDISC Standard [NCIt concept]
- Carry-Over Effect [NCIt concept]
- Case Report Form [NCIt concept]
- Case Report Form Data [NCIt concept]
- Case Report Tabulation [NCIt concept]
- Case-Control Study [NCIt concept]
- Categorical Data [NCIt concept]
- Causality Assessment [NCIt concept]
- Cellular Therapy [NCIt concept]
- Certified Copy [NCIt concept]
- Certified IRB Professional [NCIt concept]
- Challenge Agent [NCIt concept]
- Chemical Moiety [NCIt concept]
- Clean Database [NCIt concept]
- Clean File [NCIt concept]
- Client Computer [NCIt concept]
- Clinical Benefit [NCIt concept]
- Clinical Clarification [NCIt concept]
- Clinical Coordinator [NCIt concept]
- Clinical Data [NCIt concept]
- Clinical Data Sharing [NCIt concept]
- Clinical Development Plan [NCIt concept]
- Clinical Document [NCIt concept]
- Clinical Document Architecture [NCIt concept]
- Clinical Encounter [NCIt concept]
- Clinical Equipoise [NCIt concept]
- Clinical Generalizability [NCIt concept]
- Clinical Intervention or Procedure [NCIt concept]
- Clinical Investigation [NCIt concept]
- Clinical Item [NCIt concept]
- Clinical Laboratory [NCIt concept]
- Clinical Monitoring Plan [NCIt concept]
- Clinical Observation [NCIt concept]
- Clinical Outcome Assessment [NCIt concept]
- Clinical Outcome Assessment Construct Validation [NCIt concept]
- Clinical Outcome Assessment Content Validation [NCIt concept]
- Clinical Outcome Assessment Criterion Validation [NCIt concept]
- Clinical Outcomes Assessment Concept of Interest [NCIt concept]
- Clinical Outcomes Assessment Context of Use [NCIt concept]
- Clinical Pharmacology [NCIt concept]
- Clinical Research Associate [NCIt concept]
- Clinical Research and Development [NCIt concept]
- Clinical Significance [NCIt concept]
- Clinical Study [NCIt concept]
- Clinical Study Anchor [NCIt concept]
- Clinical Study Data Element [NCIt concept]
- Clinical Study Functional Role [NCIt concept]
- Clinical Study Report [NCIt concept]
- Clinical Study Report Synopsis [NCIt concept]
- Clinical Study Sponsor [NCIt concept]
- Clinical Study Subject [NCIt concept]
- Clinical Trial [NCIt concept]
- Clinical Trial Authorization [NCIt concept]
- Clinical Trial Data [NCIt concept]
- Clinical Trial Design Configuration [NCIt concept]
- Clinical Trial Development Plan [NCIt concept]
- Clinical Trial Dropout [NCIt concept]
- Clinical Trial Eligibility Criteria [NCIt concept]
- Clinical Trial Epoch [NCIt concept]
- Clinical Trial Exemption [NCIt concept]
- Clinical Trial Final Report [NCIt concept]
- Clinical Trial Information [NCIt concept]
- Clinical Trial Inspection [NCIt concept]
- Clinical Trial Interim Analysis Output Documentation [NCIt concept]
- Clinical Trial Material [NCIt concept]
- Clinical Trial Objective [NCIt concept]
- Clinical Trial Protocol [NCIt concept]
- Clinical Trial Registry [NCIt concept]
- Clinical Trial Results Registry [NCIt concept]
- Clinical Trial Site [NCIt concept]
- Clinical Trial Subject Unique Identifier [NCIt concept]
- Clinical Trial Suspension [NCIt concept]
- Clinical Trial Temporary Halt [NCIt concept]
- Clinician-reported Outcome [NCIt concept]
- Co-packaged Product [NCIt concept]
- Codelist [NCIt concept]
- Cognitive Debriefing [NCIt concept]
- Cohort [NCIt concept]
- Cohort Study [NCIt concept]
- Combination Product [NCIt concept]
- Commercially Confidential Information [NCIt concept]
- Common Data Element [NCIt concept]
- Common Terminology Criteria for Adverse Events [NCIt concept]
- Comparative Effectiveness Research [NCIt concept]
- Comparative Study [NCIt concept]
- Comparator [NCIt concept]
- Compassionate Treatment [NCIt concept]
- Compendial Name [NCIt concept]
- Completed Clinical Study [NCIt concept]
- Computer Application [NCIt concept]
- Computer Program [NCIt concept]
- Computer Programming Object Attribute [NCIt concept]
- Computer System or Software Supplier [NCIt concept]
- Concept [NCIt concept]
- Concept Unique Identifier [NCIt concept]
- Concerned Member State [NCIt concept]
- Confidence Interval [NCIt concept]
- Confidentiality [NCIt concept]
- Confirmatory Trial [NCIt concept]
- Conformity Assessment [NCIt concept]
- Confounding Variable [NCIt concept]
- Consent Form [NCIt concept]
- Consolidated Health Informatics [NCIt concept]
- Consumer Safety Officer [NCIt concept]
- Content Validity [NCIt concept]
- Contingent Subject Trial Contact [NCIt concept]
- Contract Research Organization [NCIt concept]
- Contractual Agreement [NCIt concept]
- Control Group [NCIt concept]
- Control of Electronic Records [NCIt concept]
- Controlled Study [NCIt concept]
- Controlled Vocabulary [NCIt concept]
- Coordinating Committee [NCIt concept]
- Coordinating Investigator [NCIt concept]
- Correlation [NCIt concept]
- Cross-Sectional Study [NCIt concept]
- Cross-labeled Product [NCIt concept]
- Crossover Study [NCIt concept]
- Cumulative Dose [NCIt concept]
- Cumulative Enrollment [NCIt concept]
- Current Enrollment [NCIt concept]
- Curriculum Vitae [NCIt concept]
- Daily Living [NCIt concept]
- Data [NCIt concept]
- Data Acquisition [NCIt concept]
- Data Capture [NCIt concept]
- Data Clarification [NCIt concept]
- Data Clarification Form [NCIt concept]
- Data Collection [NCIt concept]
- Data Collection Instrument [NCIt concept]
- Data Discrepancy [NCIt concept]
- Data Element [NCIt concept]
- Data Element Identifier [NCIt concept]
- Data Encryption Standard [NCIt concept]
- Data Entry [NCIt concept]
- Data Field [NCIt concept]
- Data Integrity [NCIt concept]
- Data Integrity Verification [NCIt concept]
- Data Interchange [NCIt concept]
- Data Item [NCIt concept]
- Data Item Query [NCIt concept]
- Data Item Query Management [NCIt concept]
- Data Item Query Resolution [NCIt concept]
- Data Listing [NCIt concept]
- Data Management [NCIt concept]
- Data Management Convention [NCIt concept]
- Data Mapping [NCIt concept]
- Data Message [NCIt concept]
- Data Model [NCIt concept]
- Data Monitoring [NCIt concept]
- Data Monitoring Committee [NCIt concept]
- Data Originator [NCIt concept]
- Data Quality [NCIt concept]
- Data Security [NCIt concept]
- Data Selection Criteria [NCIt concept]
- Data Set [NCIt concept]
- Data Source [NCIt concept]
- Data Standard [NCIt concept]
- Data Storage [NCIt concept]
- Data Subject [NCIt concept]
- Data Submission Model [NCIt concept]
- Data Traceability [NCIt concept]
- Data Transcription [NCIt concept]
- Data Transformation [NCIt concept]
- Data Transmission [NCIt concept]
- Data Type [NCIt concept]
- Data Validation [NCIt concept]
- Data Verification [NCIt concept]
- Database [NCIt concept]
- Database Frozen [NCIt concept]
- Database Lock [NCIt concept]
- Date of First Enrollment into Study [NCIt concept]
- De-identified Information [NCIt concept]
- Decentralized Clinical Trial [NCIt concept]
- Decision Rule [NCIt concept]
- Declaration of Helsinki [NCIt concept]
- Deep Learning [NCIt concept]
- Define.xml [NCIt concept]
- Deidentification [NCIt concept]
- Demographic Data [NCIt concept]
- Dependent Variable [NCIt concept]
- Derived Variable [NCIt concept]
- Development International Birth Date [NCIt concept]
- Device Manufacture [NCIt concept]
- Device Software Verification Evaluation Method [NCIt concept]
- Device Use Error [NCIt concept]
- Diagnosis Assessment [NCIt concept]
- Diagnostic Device [NCIt concept]
- Diagnostic Sensitivity [NCIt concept]
- Diagnostic Specificity [NCIt concept]
- Digital Signature [NCIt concept]
- Direct Access [NCIt concept]
- Direct Data Entry [NCIt concept]
- Direct Identifier [NCIt concept]
- Disease or Disorder [NCIt concept]
- Disease-Free Survival [NCIt concept]
- Document [NCIt concept]
- Document Legally Authenticated [NCIt concept]
- Document Type Definition [NCIt concept]
- Domain [NCIt concept]
- Domain Name [NCIt concept]
- Dosage Regimen [NCIt concept]
- Dose [NCIt concept]
- Dose Strength [NCIt concept]
- Double Blind Study [NCIt concept]
- Double-Dummy [NCIt concept]
- Drug Development Process [NCIt concept]
- Drug Interaction [NCIt concept]
- Drug Manufacturer [NCIt concept]
- Dynamic Hypertext Markup Language [NCIt concept]
- Early Termination of Trial [NCIt concept]
- Edit Check [NCIt concept]
- Effect Size Measurement [NCIt concept]
- Effectiveness [NCIt concept]
- Efficacy [NCIt concept]
- Electronic Case Report Form [NCIt concept]
- Electronic Case Report Tabulation [NCIt concept]
- Electronic Certified Copy [NCIt concept]
- Electronic Clinical Trial [NCIt concept]
- Electronic Consent Form [NCIt concept]
- Electronic Data Capture [NCIt concept]
- Electronic Data Capture Activation [NCIt concept]
- Electronic Data Transfer [NCIt concept]
- Electronic Document Room [NCIt concept]
- Electronic Health Record [NCIt concept]
- Electronic Medical Record [NCIt concept]
- Electronic Patient-reported Outcome System [NCIt concept]
- Electronic Personal Health Record [NCIt concept]
- Electronic Record [NCIt concept]
- Electronic Signature [NCIt concept]
- Electronic Source Data [NCIt concept]
- Electronic Source Document [NCIt concept]
- Electronic Source Record [NCIt concept]
- Electronic Source Report Form [NCIt concept]
- Electronic System Deployment [NCIt concept]
- Emergency Use Authorization [NCIt concept]
- Encode [NCIt concept]
- End Point [NCIt concept]
- End-point Assessment Medicinal Product [NCIt concept]
- Endemic Disorder [NCIt concept]
- Enrollment [NCIt concept]
- Entity With Role in Clinical Study [NCIt concept]
- Epidemic Disorder [NCIt concept]
- Equivalence Trial [NCIt concept]
- Equivalent Effect [NCIt concept]
- Essential Trial Document [NCIt concept]
- Established Drug Name [NCIt concept]
- Estimand [NCIt concept]
- Ethics Committee [NCIt concept]
- Ethnic Group [NCIt concept]
- European Harmonized Standard [NCIt concept]
- European Medicines Agency [NCIt concept]
- European Union Competent Authority [NCIt concept]
- European Union Notified Body [NCIt concept]
- Evaluable for Safety and Efficacy [NCIt concept]
- Exclusion Criteria [NCIt concept]
- Excretion [NCIt concept]
- Expansion Cohort Trial [NCIt concept]
- Expected Adverse Event [NCIt concept]
- Experimental Unit [NCIt concept]
- Exploratory Investigational New Drug Study [NCIt concept]
- Exposure [NCIt concept]
- Extensible Markup Language [NCIt concept]
- Extensible Markup Language Data Element [NCIt concept]
- Extent of Exposure [NCIt concept]
- Extraction Transformation Load [NCIt concept]
- FDA Action Letter [NCIt concept]
- FDA Approvable Letter [NCIt concept]
- FDA Clinical Outcome Assessment Qualification [NCIt concept]
- FDA Memorandum of Understanding [NCIt concept]
- FDA Not Approvable Letter [NCIt concept]
- FDA Regulation Preamble [NCIt concept]
- FDA Warning Letter [NCIt concept]
- False Negative [NCIt concept]
- False Positive [NCIt concept]
- Feels [NCIt concept]
- File Transfer Protocol [NCIt concept]
- Finding [NCIt concept]
- Finished Pharmaceutical Product [NCIt concept]
- First Subject In Date Time [NCIt concept]
- First Subject In Identity [NCIt concept]
- First Subject Screened Date Time [NCIt concept]
- First Subject Screened Identity [NCIt concept]
- First Subject Treated Date Time [NCIt concept]
- First Subject Treated Identity [NCIt concept]
- First-in-Human Study [NCIt concept]
- Follow-Up Period [NCIt concept]
- Food and Drug Administration [NCIt concept]
- Form [NCIt concept]
- Frequentist Method [NCIt concept]
- Gender [NCIt concept]
- Gene Therapy [NCIt concept]
- Generic Name [NCIt concept]
- Global Assessment Variable [NCIt concept]
- Glossary [NCIt concept]
- Good Clinical Practice [NCIt concept]
- Granularity [NCIt concept]
- Group Sequential Design [NCIt concept]
- HL7 Document [NCIt concept]
- HTML Browser [NCIt concept]
- Handwritten Signature [NCIt concept]
- Health Care Provider [NCIt concept]
- Health Information Exchange [NCIt concept]
- Health Level Seven [NCIt concept]
- Health Literacy [NCIt concept]
- Health-related Quality of Life [NCIt concept]
- Healthcare Facility [NCIt concept]
- Healthy Subject [NCIt concept]
- Hereditary [NCIt concept]
- Human Study Subject [NCIt concept]
- Huriet Law [NCIt concept]
- Hypertext [NCIt concept]
- Hypertext Markup Language [NCIt concept]
- Hypothesis To Test [NCIt concept]
- ICH Common Technical Document [NCIt concept]
- ICH Type Of Comparison [NCIt concept]
- Immediately Life-Threatening Disorder [NCIt concept]
- Impartial Witness [NCIt concept]
- Importance Weight [NCIt concept]
- In Vitro Diagnostic Device [NCIt concept]
- Incidence [NCIt concept]
- Incidence Rate [NCIt concept]
- Inclusion Criteria [NCIt concept]
- Independent Data Monitoring Committee [NCIt concept]
- Independent Ethics Committee [NCIt concept]
- Independent Ethics Committee Opinion [NCIt concept]
- Independent Variable [NCIt concept]
- Indication [NCIt concept]
- Indirect Identifier [NCIt concept]
- Individual Exposure [NCIt concept]
- Informed Consent [NCIt concept]
- Infusion Procedure [NCIt concept]
- Institutional Review Board [NCIt concept]
- Institutional Review Board Approval [NCIt concept]
- Intent To Treat [NCIt concept]
- Inter-rater Reliability [NCIt concept]
- Intercurrent Event [NCIt concept]
- Interim Analysis [NCIt concept]
- Interim Analysis Schedule [NCIt concept]
- Internal Consistency [NCIt concept]
- International Marketing Authorization Birth Date [NCIt concept]
- International Nonproprietary Name [NCIt concept]
- Internet [NCIt concept]
- Internet Service Provider [NCIt concept]
- Interoperability [NCIt concept]
- Intra Subject Variability [NCIt concept]
- Investigational Brochure [NCIt concept]
- Investigational Medical Device [NCIt concept]
- Investigational Medicinal Product [NCIt concept]
- Investigational Subject Case History [NCIt concept]
- Investigator [NCIt concept]
- Investigator Recruitment Process [NCIt concept]
- Investigator/Institution [NCIt concept]
- Item Definition [NCIt concept]
- Item Group Definition [NCIt concept]
- Janus Clinical Trials Repository Model [NCIt concept]
- Janus Study Data Repository [NCIt concept]
- Labeling [NCIt concept]
- Last Subject In Date Time [NCIt concept]
- Last Subject In Identity [NCIt concept]
- Last Subject Last Visit Date Time [NCIt concept]
- Last Subject Last Visit Identity [NCIt concept]
- Legally Acceptable Representative [NCIt concept]
- Life Threatening Adverse Event [NCIt concept]
- Long-term Follow-up [NCIt concept]
- Longitudinal Study [NCIt concept]
- Low-interventional Clinical Trial [NCIt concept]
- Machine Learning [NCIt concept]
- Marketing Authorization [NCIt concept]
- Marketing Authorization Holder [NCIt concept]
- Marketing Authorization Procedure [NCIt concept]
- Marketing Support Trials [NCIt concept]
- Markup [NCIt concept]
- Masking [NCIt concept]
- Master Protocol [NCIt concept]
- Matched-Pair Design [NCIt concept]
- MedDRA [NCIt concept]
- Median [NCIt concept]
- Medical Countermeasure [NCIt concept]
- Medical Device [NCIt concept]
- Medical Monitor [NCIt concept]
- Medical Product Label [NCIt concept]
- Medical Product or Procedure Intent of Use [NCIt concept]
- Medication [NCIt concept]
- Medication Error [NCIt concept]
- Medicinal Product [NCIt concept]
- Medicinal Product Classification [NCIt concept]
- Medicinal Product Identifier [NCIt concept]
- Medicinal Product Name [NCIt concept]
- Medicines And Healthcare Products Regulatory Agency [NCIt concept]
- Mega-Trial [NCIt concept]
- Memory Cache [NCIt concept]
- Meta-Analysis [NCIt concept]
- Meta-Analysis Protocol Document [NCIt concept]
- Metabolic Process [NCIt concept]
- Metadata [NCIt concept]
- Minor Person [NCIt concept]
- Missing Data [NCIt concept]
- Mode [NCIt concept]
- Model [NCIt concept]
- Modem Device [NCIt concept]
- Monitoring [NCIt concept]
- Morbidity [NCIt concept]
- Morbidity Rate [NCIt concept]
- Mortality Rate [NCIt concept]
- Multi-Institutional Clinical Trial [NCIt concept]
- Mutual Recognition Procedure [NCIt concept]
- N-of-1 Trial [NCIt concept]
- NCI Enterprise Vocabulary Services [NCIt concept]
- Natural Language [NCIt concept]
- Natural Language Processing [NCIt concept]
- Negative Test Result [NCIt concept]
- New Chemical Entity [NCIt concept]
- New Drug Application [NCIt concept]
- New Molecular Entity [NCIt concept]
- New Safety Information [NCIt concept]
- No Observable Effect Level [NCIt concept]
- Nomenclature [NCIt concept]
- Non-Inferiority Trial [NCIt concept]
- Non-Interventional Study [NCIt concept]
- Non-confirmatory Result [NCIt concept]
- Nonclinical Study [NCIt concept]
- Null Hypothesis [NCIt concept]
- Nuremberg Code [NCIt concept]
- Object Class [NCIt concept]
- Observational Study [NCIt concept]
- Observer Assessment [NCIt concept]
- Observer-reported Outcome [NCIt concept]
- Off-label [NCIt concept]
- Official Protocol Title [NCIt concept]
- Ontology [NCIt concept]
- Open Label Study [NCIt concept]
- Open To Enrollment [NCIt concept]
- Operational Model [NCIt concept]
- Original Data [NCIt concept]
- Other Medically Important Serious Event [NCIt concept]
- Outcome [NCIt concept]
- Outcomes Research [NCIt concept]
- Outlier [NCIt concept]
- Overdose [NCIt concept]
- P-Value [NCIt concept]
- Packaging Materials [NCIt concept]
- Pairing [NCIt concept]
- Pandemic Disorder [NCIt concept]
- Paper Case Report Form [NCIt concept]
- Parallel Study [NCIt concept]
- Parameter [NCIt concept]
- Password Aging [NCIt concept]
- Patient [NCIt concept]
- Patient File [NCIt concept]
- Patient Monitoring [NCIt concept]
- Patient Reported Outcome [NCIt concept]
- Patient Reported Outcome Stem [NCIt concept]
- Patient Reported Outcomes Measurement Information System [NCIt concept]
- Patient Self-Report [NCIt concept]
- Patient-Reported Outcome Item Generation [NCIt concept]
- Patient-Reported Survey Instrument [NCIt concept]
- Patient-reported Outcome Item [NCIt concept]
- Peer Review [NCIt concept]
- Per-Protocol Analysis Set [NCIt concept]
- Performance Outcome [NCIt concept]
- Performed Clinical Study Activity [NCIt concept]
- Period Effect [NCIt concept]
- Permanent Data [NCIt concept]
- Permissible Value [NCIt concept]
- Personal Information [NCIt concept]
- Pharmaceutical Dosage Form [NCIt concept]
- Pharmaceutical Product Ingredient [NCIt concept]
- Pharmacodynamics [NCIt concept]
- Pharmacoeconomics [NCIt concept]
- Pharmacogenetic Test [NCIt concept]
- Pharmacogenetics [NCIt concept]
- Pharmacogenomic Test [NCIt concept]
- Pharmacogenomics [NCIt concept]
- Pharmacokinetics [NCIt concept]
- Pharmacokinetics: Distribution [NCIt concept]
- Pharmacologic Substance [NCIt concept]
- Pharmacology [NCIt concept]
- Pharmacovigilance [NCIt concept]
- Phase 0 Trial [NCIt concept]
- Phase I Trial [NCIt concept]
- Phase II Trial [NCIt concept]
- Phase III Trial [NCIt concept]
- Phase IIIb Trial [NCIt concept]
- Phase IIa Trial [NCIt concept]
- Phase IIb Trial [NCIt concept]
- Phase IV Trial [NCIt concept]
- Phase V Trial [NCIt concept]
- Phlebotomy [NCIt concept]
- Placebo [NCIt concept]
- Placebo-Controlled Trial [NCIt concept]
- Plain Language Writing [NCIt concept]
- Planned Subject Number [NCIt concept]
- Planned Trial Subject Contact [NCIt concept]
- Platform Trial [NCIt concept]
- Platform Trial Design [NCIt concept]
- Population Group [NCIt concept]
- Positive Laboratory Test Result [NCIt concept]
- Post Marketing Requirement [NCIt concept]
- Postmarketing Commitment [NCIt concept]
- Postmarketing Surveillance [NCIt concept]
- Pragmatic Trial [NCIt concept]
- Pre-market Approval Application [NCIt concept]
- Preclinical Study [NCIt concept]
- Premarket Device Notification [NCIt concept]
- Prevalence [NCIt concept]
- Preventive Intervention [NCIt concept]
- Primary Completion Date [NCIt concept]
- Primary Outcome Variable [NCIt concept]
- Principal Investigator [NCIt concept]
- Privacy Breach [NCIt concept]
- Probability [NCIt concept]
- Product Dose [NCIt concept]
- Prognostic Covariate [NCIt concept]
- Progression-free Survival [NCIt concept]
- Proprietary Name [NCIt concept]
- Prospective Study [NCIt concept]
- Protected Personal Data [NCIt concept]
- Protocol Agent [NCIt concept]
- Protocol Amendment [NCIt concept]
- Protocol Approval by Sponsor [NCIt concept]
- Protocol Background Material [NCIt concept]
- Protocol Deviation [NCIt concept]
- Protocol Event [NCIt concept]
- Protocol Identifier [NCIt concept]
- Protocol Referenced Documents [NCIt concept]
- Protocol Title [NCIt concept]
- Protocol Violation [NCIt concept]
- Proxy Data Origin [NCIt concept]
- Proxy Respondent [NCIt concept]
- Proxy-reported Outcome [NCIt concept]
- Pseudonymization [NCIt concept]
- Psychometric Instrument Reliability [NCIt concept]
- Psychometric Validation [NCIt concept]
- Psychometrics [NCIt concept]
- Qualitative Variable [NCIt concept]
- Quality Assurance [NCIt concept]
- Quality Control [NCIt concept]
- Quality of Life [NCIt concept]
- Quantitative Variable [NCIt concept]
- Questionnaire [NCIt concept]
- Race [NCIt concept]
- Radiopharmaceutical Medicinal Product [NCIt concept]
- Random Allocation [NCIt concept]
- Random Number Table [NCIt concept]
- Random Sample Population [NCIt concept]
- Randomization [NCIt concept]
- Randomized Controlled Clinical Trial [NCIt concept]
- Raw Data [NCIt concept]
- Real-world Data [NCIt concept]
- Real-world Evidence [NCIt concept]
- Record [NCIt concept]
- Recruitment [NCIt concept]
- Recruitment Period [NCIt concept]
- Recruitment Target [NCIt concept]
- Reference Information Model [NCIt concept]
- Reference Member State [NCIt concept]
- Regenerative Medical Therapy [NCIt concept]
- Regenerative Medicine [NCIt concept]
- Regenerative Medicine Advanced Therapy Designation [NCIt concept]
- Regional Health Information Organization [NCIt concept]
- Regulated Clinical Research and Information Management [NCIt concept]
- Regulatory Application [NCIt concept]
- Regulatory Authority [NCIt concept]
- Remote Clinical Trial [NCIt concept]
- Repeat Activity Until Rule [NCIt concept]
- Report [NCIt concept]
- Rescue Medications [NCIt concept]
- Research Hypothesis [NCIt concept]
- Residual Risk [NCIt concept]
- Response Option [NCIt concept]
- Results Posting [NCIt concept]
- Results Posting Date [NCIt concept]
- Retrospective Data Capture [NCIt concept]
- Retrospective Study [NCIt concept]
- Risk Based Monitoring [NCIt concept]
- Route of Administration [NCIt concept]
- SAFE-Biopharma Standard [NCIt concept]
- Safety [NCIt concept]
- Safety and Tolerability [NCIt concept]
- Sample Size [NCIt concept]
- Sample Size Adjustment [NCIt concept]
- Sample Size Calculation [NCIt concept]
- Schedule Of Assessments [NCIt concept]
- Schedule of Activities [NCIt concept]
- Screening Epoch [NCIt concept]
- Screening Study [NCIt concept]
- Script [NCIt concept]
- Secondary Outcome Variable [NCIt concept]
- Secondary Sponsor [NCIt concept]
- Self-Evident Change [NCIt concept]
- Semantic Interoperability [NCIt concept]
- Semantics [NCIt concept]
- Sensitive Data [NCIt concept]
- Serious Adverse Drug Reaction [NCIt concept]
- Serious Adverse Event [NCIt concept]
- Serious Adverse Experience [NCIt concept]
- Serious Breach [NCIt concept]
- Serious Risk [NCIt concept]
- Server [NCIt concept]
- Severe [NCIt concept]
- Sex [NCIt concept]
- Side Effect [NCIt concept]
- Sign [NCIt concept]
- Signal of a Serious Risk [NCIt concept]
- Single Blind Study [NCIt concept]
- Single-entity Product [NCIt concept]
- Site Investigator [NCIt concept]
- Site Screening [NCIt concept]
- Social Circumstances [NCIt concept]
- Software Validation [NCIt concept]
- Software as a Medical Device [NCIt concept]
- Source [NCIt concept]
- Source Data [NCIt concept]
- Source Data Verification [NCIt concept]
- Source Document [NCIt concept]
- Source Document Verification [NCIt concept]
- Special Population [NCIt concept]
- Special Purpose Domain [NCIt concept]
- Specified Substance [NCIt concept]
- Sponsor-Investigator [NCIt concept]
- Standard [NCIt concept]
- Standard Deviation [NCIt concept]
- Standard Operating Procedure [NCIt concept]
- Standard Treatment [NCIt concept]
- Standard for the Exchange of Nonclinical Data [NCIt concept]
- Standards Development Organization [NCIt concept]
- Statistical Analysis Plan [NCIt concept]
- Statistical Distribution [NCIt concept]
- Statistical Power [NCIt concept]
- Statistical Significance [NCIt concept]
- Statistical Technique [NCIt concept]
- Stochastic [NCIt concept]
- Stopping Rules [NCIt concept]
- Stratification [NCIt concept]
- Structured Data [NCIt concept]
- Structured Health Record Information [NCIt concept]
- Structured Product Labeling [NCIt concept]
- Study Arm [NCIt concept]
- Study Branch [NCIt concept]
- Study Completion Date [NCIt concept]
- Study Conduct [NCIt concept]
- Study Control [NCIt concept]
- Study Data Standardization Plan [NCIt concept]
- Study Description [NCIt concept]
- Study Design [NCIt concept]
- Study Design Rationale [NCIt concept]
- Study Life Cycle [NCIt concept]
- Study Monitor [NCIt concept]
- Study Monitoring [NCIt concept]
- Study Monitoring Report [NCIt concept]
- Study Monitoring Visit [NCIt concept]
- Study Outcome Description [NCIt concept]
- Study Outcome Measurement [NCIt concept]
- Study Participant [NCIt concept]
- Study Phase [NCIt concept]
- Study Population [NCIt concept]
- Study Protocol Document Version Public Title [NCIt concept]
- Study Publication Date [NCIt concept]
- Study Reconstruction [NCIt concept]
- Study Registry [NCIt concept]
- Study Report Completion Date [NCIt concept]
- Study Results [NCIt concept]
- Study Roles and Responsibilities Table [NCIt concept]
- Study Schematic [NCIt concept]
- Study Start [NCIt concept]
- Study Start Date [NCIt concept]
- Study Subject Discontinuation [NCIt concept]
- Study Subject Enrolled [NCIt concept]
- Study Variable [NCIt concept]
- Study Visit [NCIt concept]
- Study on Hold [NCIt concept]
- Subinvestigator [NCIt concept]
- Subject Completed Participation in Study [NCIt concept]
- Subject Data Event [NCIt concept]
- Subject Monitoring [NCIt concept]
- Subject Risk [NCIt concept]
- Subject Well-Being [NCIt concept]
- Substance Screening [NCIt concept]
- Superiority Trial [NCIt concept]
- Surrogate Endpoint [NCIt concept]
- Surrogate Marker [NCIt concept]
- Surrogate Variable [NCIt concept]
- Survey [NCIt concept]
- Symptom [NCIt concept]
- Synergistic Effect [NCIt concept]
- Synopsis [NCIt concept]
- Syntax [NCIt concept]
- Synthetic Data [NCIt concept]
- System [NCIt concept]
- System Alert [NCIt concept]
- System Migration [NCIt concept]
- Systematized Nomenclature of Medicine [NCIt concept]
- Tabulation Dataset [NCIt concept]
- Target Study Population [NCIt concept]
- Technology Provider [NCIt concept]
- Term [NCIt concept]
- Terminology [NCIt concept]
- Therapeutic Area [NCIt concept]
- Therapeutic Effect [NCIt concept]
- Therapeutic Exploratory Study [NCIt concept]
- Therapeutic Index [NCIt concept]
- Therapeutic Procedure [NCIt concept]
- Titration Study [NCIt concept]
- Token [NCIt concept]
- Transition Rule [NCIt concept]
- Translation [NCIt concept]
- Translational Research [NCIt concept]
- Treatment Benefit [NCIt concept]
- Treatment Contrast Interaction [NCIt concept]
- Treatment Effect [NCIt concept]
- Treatment Efficacy [NCIt concept]
- Treatment-Emergent Adverse Event [NCIt concept]
- Trial Compliance [NCIt concept]
- Trial Design Element [NCIt concept]
- Trial Design Model [NCIt concept]
- Trial Exploratory Objective [NCIt concept]
- Trial Phase [NCIt concept]
- Trial Primary Objective [NCIt concept]
- Trial Screen Failure [NCIt concept]
- Trial Screening [NCIt concept]
- Trial Secondary Objective [NCIt concept]
- Trial Statistician [NCIt concept]
- Trial Subject Replacement [NCIt concept]
- Trial Termination [NCIt concept]
- Triple Blind Study [NCIt concept]
- Trustworthy Electronic Record [NCIt concept]
- Type 3 Error [NCIt concept]
- Umbrella Trial [NCIt concept]
- Umbrella Trial Design [NCIt concept]
- Unblinding [NCIt concept]
- Unexpected Adverse Drug Reaction [NCIt concept]
- Unexpected Serious Risk [NCIt concept]
- Uniform Resource Locator [NCIt concept]
- Use Case [NCIt concept]
- User Site Testing [NCIt concept]
- Vaccine [NCIt concept]
- Vaccine Effectiveness [NCIt concept]
- Vaccine Efficacy [NCIt concept]
- Valid [NCIt concept]
- Validation [NCIt concept]
- Variable [NCIt concept]
- Variance [NCIt concept]
- Verification [NCIt concept]
- Virtual [NCIt concept]
- Virulence [NCIt concept]
- Vocabulary [NCIt concept]
- Vulnerable Subjects [NCIt concept]
- Washout Period [NCIt concept]
- Web Browser [NCIt concept]
- Web Page [NCIt concept]
- Web Server [NCIt concept]
- Web Site [NCIt concept]
- Withdrawal by Subject [NCIt concept]
- World Wide Web [NCIt concept]
- XML Document Root [NCIt concept]
- Zoonotic Infection [NCIt concept]
- t-Test [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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